SNP Links for Gene (Select 3116) - SNP

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Select item 14914773211.

rs1491477321 has merged into rs9280336 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTTTTTTT>-,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 6:33127433 (GRCh38)
6:33095210 (GRCh37)
Canonical SPDI:: NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTT=0./0 (ALFA)
TTTTTTTTTTTTTTTT=0./0 (GENOME_DK)
HGVS:: NC_000006.12:g.33127433_33127452del, NC_000006.12:g.33127436_33127452del, NC_000006.12:g.33127437_33127452del, NC_000006.12:g.33127438_33127452del, NC_000006.12:g.33127439_33127452del, NC_000006.12:g.33127440_33127452del, NC_000006.12:g.33127441_33127452del, NC_000006.12:g.33127442_33127452del, NC_000006.12:g.33127443_33127452del, NC_000006.12:g.33127444_33127452del, NC_000006.12:g.33127445_33127452del, NC_000006.12:g.33127446_33127452del, NC_000006.12:g.33127447_33127452del, NC_000006.12:g.33127448_33127452del, NC_000006.12:g.33127449_33127452del, NC_000006.12:g.33127450_33127452del, NC_000006.12:g.33127451_33127452del, NC_000006.12:g.33127452del, NC_000006.12:g.33127452dup, NC_000006.12:g.33127451_33127452dup, NC_000006.12:g.33127450_33127452dup, NC_000006.12:g.33127449_33127452dup, NC_000006.12:g.33127448_33127452dup, NC_000006.12:g.33127447_33127452dup, NC_000006.12:g.33127446_33127452dup, NC_000006.12:g.33127445_33127452dup, NC_000006.12:g.33127444_33127452dup, NC_000006.12:g.33127443_33127452dup, NC_000006.12:g.33127442_33127452dup, NC_000006.12:g.33127441_33127452dup, NC_000006.12:g.33127440_33127452dup, NC_000006.12:g.33127435_33127452dup, NC_000006.12:g.33127430_33127452dup, NC_000006.12:g.33127427_33127452dup, NC_000006.12:g.33127452_33127453insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.33127452_33127453insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.33127452_33127453insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.33095210_33095229del, NC_000006.11:g.33095213_33095229del, NC_000006.11:g.33095214_33095229del, NC_000006.11:g.33095215_33095229del, NC_000006.11:g.33095216_33095229del, NC_000006.11:g.33095217_33095229del, NC_000006.11:g.33095218_33095229del, NC_000006.11:g.33095219_33095229del, NC_000006.11:g.33095220_33095229del, NC_000006.11:g.33095221_33095229del, NC_000006.11:g.33095222_33095229del, NC_000006.11:g.33095223_33095229del, NC_000006.11:g.33095224_33095229del, NC_000006.11:g.33095225_33095229del, NC_000006.11:g.33095226_33095229del, NC_000006.11:g.33095227_33095229del, NC_000006.11:g.33095228_33095229del, NC_000006.11:g.33095229del, NC_000006.11:g.33095229dup, NC_000006.11:g.33095228_33095229dup, NC_000006.11:g.33095227_33095229dup, NC_000006.11:g.33095226_33095229dup, NC_000006.11:g.33095225_33095229dup, NC_000006.11:g.33095224_33095229dup, NC_000006.11:g.33095223_33095229dup, NC_000006.11:g.33095222_33095229dup, NC_000006.11:g.33095221_33095229dup, NC_000006.11:g.33095220_33095229dup, NC_000006.11:g.33095219_33095229dup, NC_000006.11:g.33095218_33095229dup, NC_000006.11:g.33095217_33095229dup, NC_000006.11:g.33095212_33095229dup, NC_000006.11:g.33095207_33095229dup, NC_000006.11:g.33095204_33095229dup, NC_000006.11:g.33095229_33095230insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.33095229_33095230insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.33095229_33095230insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.3:g.4538909_4538911dup, NT_113891.3:g.4538895_4538911del, NT_113891.3:g.4538898_4538911del, NT_113891.3:g.4538899_4538911del, NT_113891.3:g.4538900_4538911del, NT_113891.3:g.4538901_4538911del, NT_113891.3:g.4538902_4538911del, NT_113891.3:g.4538903_4538911del, NT_113891.3:g.4538904_4538911del, NT_113891.3:g.4538905_4538911del, NT_113891.3:g.4538906_4538911del, NT_113891.3:g.4538907_4538911del, NT_113891.3:g.4538908_4538911del, NT_113891.3:g.4538909_4538911del, NT_113891.3:g.4538910_4538911del, NT_113891.3:g.4538911del, NT_113891.3:g.4538911dup, NT_113891.3:g.4538910_4538911dup, NT_113891.3:g.4538908_4538911dup, NT_113891.3:g.4538907_4538911dup, NT_113891.3:g.4538906_4538911dup, NT_113891.3:g.4538905_4538911dup, NT_113891.3:g.4538904_4538911dup, NT_113891.3:g.4538903_4538911dup, NT_113891.3:g.4538902_4538911dup, NT_113891.3:g.4538901_4538911dup, NT_113891.3:g.4538900_4538911dup, NT_113891.3:g.4538899_4538911dup, NT_113891.3:g.4538898_4538911dup, NT_113891.3:g.4538897_4538911dup, NT_113891.3:g.4538896_4538911dup, NT_113891.3:g.4538891_4538911dup, NT_113891.3:g.4538911_4538912insTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.3:g.4538911_4538912insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.3:g.4538911_4538912insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.3:g.4538911_4538912insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.3:g.4538911_4538912insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.4321790_4321803dup, NT_167248.2:g.4321798_4321803del, NT_167248.2:g.4321801_4321803del, NT_167248.2:g.4321802_4321803del, NT_167248.2:g.4321803del, NT_167248.2:g.4321803dup, NT_167248.2:g.4321802_4321803dup, NT_167248.2:g.4321801_4321803dup, NT_167248.2:g.4321800_4321803dup, NT_167248.2:g.4321799_4321803dup, NT_167248.2:g.4321798_4321803dup, NT_167248.2:g.4321797_4321803dup, NT_167248.2:g.4321796_4321803dup, NT_167248.2:g.4321795_4321803dup, NT_167248.2:g.4321794_4321803dup, NT_167248.2:g.4321793_4321803dup, NT_167248.2:g.4321792_4321803dup, NT_167248.2:g.4321791_4321803dup, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTT, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTTT, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTTTT, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTTTTT, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.2:g.4576092_4576096dup, NT_167249.2:g.4576082_4576096del, NT_167249.2:g.4576085_4576096del, NT_167249.2:g.4576086_4576096del, NT_167249.2:g.4576087_4576096del, NT_167249.2:g.4576088_4576096del, NT_167249.2:g.4576089_4576096del, NT_167249.2:g.4576090_4576096del, NT_167249.2:g.4576091_4576096del, NT_167249.2:g.4576092_4576096del, NT_167249.2:g.4576093_4576096del, NT_167249.2:g.4576094_4576096del, NT_167249.2:g.4576095_4576096del, NT_167249.2:g.4576096del, NT_167249.2:g.4576096dup, NT_167249.2:g.4576095_4576096dup, NT_167249.2:g.4576094_4576096dup, NT_167249.2:g.4576093_4576096dup, NT_167249.2:g.4576091_4576096dup, NT_167249.2:g.4576090_4576096dup, NT_167249.2:g.4576089_4576096dup, NT_167249.2:g.4576088_4576096dup, NT_167249.2:g.4576087_4576096dup, NT_167249.2:g.4576086_4576096dup, NT_167249.2:g.4576085_4576096dup, NT_167249.2:g.4576084_4576096dup, NT_167249.2:g.4576083_4576096dup, NT_167249.2:g.4576082_4576096dup, NT_167249.2:g.4576081_4576096dup, NT_167249.2:g.4576080_4576096dup, NT_167249.2:g.4576079_4576096dup, NT_167249.2:g.4576074_4576096dup, NT_167249.2:g.4576096_4576097insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.2:g.4576096_4576097insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.2:g.4576096_4576097insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.2:g.4576096_4576097insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.2:g.4576096_4576097insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.4546859_4546872dup, NT_167246.2:g.4546867_4546872del, NT_167246.2:g.4546870_4546872del, NT_167246.2:g.4546871_4546872del, NT_167246.2:g.4546872del, NT_167246.2:g.4546872dup, NT_167246.2:g.4546871_4546872dup, NT_167246.2:g.4546870_4546872dup, NT_167246.2:g.4546869_4546872dup, NT_167246.2:g.4546868_4546872dup, NT_167246.2:g.4546867_4546872dup, NT_167246.2:g.4546866_4546872dup, NT_167246.2:g.4546865_4546872dup, NT_167246.2:g.4546864_4546872dup, NT_167246.2:g.4546863_4546872dup, NT_167246.2:g.4546862_4546872dup, NT_167246.2:g.4546861_4546872dup, NT_167246.2:g.4546860_4546872dup, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTT, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTTT, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTTTT, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTTTTT, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167244.2:g.4432048C>T, NT_167244.2:g.4432048_4432067del, NT_167244.2:g.4432048_4432064del, NT_167244.2:g.4432048_4432063del, NT_167244.2:g.4432048_4432062del, NT_167244.2:g.4432048_4432061del, NT_167244.2:g.4432048_4432060del, NT_167244.2:g.4432048_4432059del, NT_167244.2:g.4432048_4432058del, NT_167244.2:g.4432048_4432057del, NT_167244.2:g.4432048_4432056del, NT_167244.2:g.4432048_4432055del, NT_167244.2:g.4432048_4432054del, NT_167244.2:g.4432048_4432053del, NT_167244.2:g.4432048_4432052del, NT_167244.2:g.4432048_4432051del, NT_167244.2:g.4432045CTT[1], NT_167244.2:g.4432048_4432049del, NT_167244.2:g.4432048del, NT_167244.2:g.4432048delinsTT, NT_167244.2:g.4432048delinsTTT, NT_167244.2:g.4432048delinsTTTT, NT_167244.2:g.4432048delinsTTTTT, NT_167244.2:g.4432048delinsTTTTTT, NT_167244.2:g.4432048delinsTTTTTTT, NT_167244.2:g.4432048delinsTTTTTTTT, NT_167244.2:g.4432048delinsTTTTTTTTT, NT_167244.2:g.4432048delinsTTTTTTTTTT, NT_167244.2:g.4432048delinsTTTTTTTTTTT, NT_167244.2:g.4432048delinsTTTTTTTTTTTT, NT_167244.2:g.4432048delinsTTTTTTTTTTTTT, NT_167244.2:g.4432048delinsTTTTTTTTTTTTTT, NT_167244.2:g.4432048delinsTTTTTTTTTTTTTTTTTTT, NT_167244.2:g.4432048delinsTTTTTTTTTTTTTTTTTTTTTTTT, NT_167244.2:g.4432048delinsTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167244.2:g.4432048delinsTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167244.2:g.4432048delinsTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167244.2:g.4432048delinsTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167244.1:g.4381964C>T, NT_167244.1:g.4381964_4381983del, NT_167244.1:g.4381964_4381980del, NT_167244.1:g.4381964_4381979del, NT_167244.1:g.4381964_4381978del, NT_167244.1:g.4381964_4381977del, NT_167244.1:g.4381964_4381976del, NT_167244.1:g.4381964_4381975del, NT_167244.1:g.4381964_4381974del, NT_167244.1:g.4381964_4381973del, NT_167244.1:g.4381964_4381972del, NT_167244.1:g.4381964_4381971del, NT_167244.1:g.4381964_4381970del, NT_167244.1:g.4381964_4381969del, NT_167244.1:g.4381964_4381968del, NT_167244.1:g.4381964_4381967del, NT_167244.1:g.4381961CTT[1], NT_167244.1:g.4381964_4381965del, NT_167244.1:g.4381964del, NT_167244.1:g.4381964delinsTT, NT_167244.1:g.4381964delinsTTT, NT_167244.1:g.4381964delinsTTTT, NT_167244.1:g.4381964delinsTTTTT, NT_167244.1:g.4381964delinsTTTTTT, NT_167244.1:g.4381964delinsTTTTTTT, NT_167244.1:g.4381964delinsTTTTTTTT, NT_167244.1:g.4381964delinsTTTTTTTTT, NT_167244.1:g.4381964delinsTTTTTTTTTT, NT_167244.1:g.4381964delinsTTTTTTTTTTT, NT_167244.1:g.4381964delinsTTTTTTTTTTTT, NT_167244.1:g.4381964delinsTTTTTTTTTTTTT, NT_167244.1:g.4381964delinsTTTTTTTTTTTTTT, NT_167244.1:g.4381964delinsTTTTTTTTTTTTTTTTTTT, NT_167244.1:g.4381964delinsTTTTTTTTTTTTTTTTTTTTTTTT, NT_167244.1:g.4381964delinsTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167244.1:g.4381964delinsTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167244.1:g.4381964delinsTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167244.1:g.4381964delinsTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.2:g.4539015_4539017dup, NT_113891.2:g.4539001_4539017del, NT_113891.2:g.4539004_4539017del, NT_113891.2:g.4539005_4539017del, NT_113891.2:g.4539006_4539017del, NT_113891.2:g.4539007_4539017del, NT_113891.2:g.4539008_4539017del, NT_113891.2:g.4539009_4539017del, NT_113891.2:g.4539010_4539017del, NT_113891.2:g.4539011_4539017del, NT_113891.2:g.4539012_4539017del, NT_113891.2:g.4539013_4539017del, NT_113891.2:g.4539014_4539017del, NT_113891.2:g.4539015_4539017del, NT_113891.2:g.4539016_4539017del, NT_113891.2:g.4539017del, NT_113891.2:g.4539017dup, NT_113891.2:g.4539016_4539017dup, NT_113891.2:g.4539014_4539017dup, NT_113891.2:g.4539013_4539017dup, NT_113891.2:g.4539012_4539017dup, NT_113891.2:g.4539011_4539017dup, NT_113891.2:g.4539010_4539017dup, NT_113891.2:g.4539009_4539017dup, NT_113891.2:g.4539008_4539017dup, NT_113891.2:g.4539007_4539017dup, NT_113891.2:g.4539006_4539017dup, NT_113891.2:g.4539005_4539017dup, NT_113891.2:g.4539004_4539017dup, NT_113891.2:g.4539003_4539017dup, NT_113891.2:g.4539002_4539017dup, NT_113891.2:g.4538997_4539017dup, NT_113891.2:g.4539017_4539018insTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.2:g.4539017_4539018insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.2:g.4539017_4539018insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.2:g.4539017_4539018insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.2:g.4539017_4539018insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.4327386_4327399dup, NT_167248.1:g.4327394_4327399del, NT_167248.1:g.4327397_4327399del, NT_167248.1:g.4327398_4327399del, NT_167248.1:g.4327399del, NT_167248.1:g.4327399dup, NT_167248.1:g.4327398_4327399dup, NT_167248.1:g.4327397_4327399dup, NT_167248.1:g.4327396_4327399dup, NT_167248.1:g.4327395_4327399dup, NT_167248.1:g.4327394_4327399dup, NT_167248.1:g.4327393_4327399dup, NT_167248.1:g.4327392_4327399dup, NT_167248.1:g.4327391_4327399dup, NT_167248.1:g.4327390_4327399dup, NT_167248.1:g.4327389_4327399dup, NT_167248.1:g.4327388_4327399dup, NT_167248.1:g.4327387_4327399dup, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTT, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTTT, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTTTT, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTTTTT, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.1:g.4575390_4575394dup, NT_167249.1:g.4575380_4575394del, NT_167249.1:g.4575383_4575394del, NT_167249.1:g.4575384_4575394del, NT_167249.1:g.4575385_4575394del, NT_167249.1:g.4575386_4575394del, NT_167249.1:g.4575387_4575394del, NT_167249.1:g.4575388_4575394del, NT_167249.1:g.4575389_4575394del, NT_167249.1:g.4575390_4575394del, NT_167249.1:g.4575391_4575394del, NT_167249.1:g.4575392_4575394del, NT_167249.1:g.4575393_4575394del, NT_167249.1:g.4575394del, NT_167249.1:g.4575394dup, NT_167249.1:g.4575393_4575394dup, NT_167249.1:g.4575392_4575394dup, NT_167249.1:g.4575391_4575394dup, NT_167249.1:g.4575389_4575394dup, NT_167249.1:g.4575388_4575394dup, NT_167249.1:g.4575387_4575394dup, NT_167249.1:g.4575386_4575394dup, NT_167249.1:g.4575385_4575394dup, NT_167249.1:g.4575384_4575394dup, NT_167249.1:g.4575383_4575394dup, NT_167249.1:g.4575382_4575394dup, NT_167249.1:g.4575381_4575394dup, NT_167249.1:g.4575380_4575394dup, NT_167249.1:g.4575379_4575394dup, NT_167249.1:g.4575378_4575394dup, NT_167249.1:g.4575377_4575394dup, NT_167249.1:g.4575372_4575394dup, NT_167249.1:g.4575394_4575395insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.1:g.4575394_4575395insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.1:g.4575394_4575395insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.1:g.4575394_4575395insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.1:g.4575394_4575395insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.4552479_4552492dup, NT_167246.1:g.4552487_4552492del, NT_167246.1:g.4552490_4552492del, NT_167246.1:g.4552491_4552492del, NT_167246.1:g.4552492del, NT_167246.1:g.4552492dup, NT_167246.1:g.4552491_4552492dup, NT_167246.1:g.4552490_4552492dup, NT_167246.1:g.4552489_4552492dup, NT_167246.1:g.4552488_4552492dup, NT_167246.1:g.4552487_4552492dup, NT_167246.1:g.4552486_4552492dup, NT_167246.1:g.4552485_4552492dup, NT_167246.1:g.4552484_4552492dup, NT_167246.1:g.4552483_4552492dup, NT_167246.1:g.4552482_4552492dup, NT_167246.1:g.4552481_4552492dup, NT_167246.1:g.4552480_4552492dup, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTT, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTTT, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTTTT, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTTTTT, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 14913388042.

rs1491338804 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CT [Show Flanks]
Chromosome:: 6:33127425 (GRCh38)
6:33095203 (GRCh37)
Canonical SPDI:: NC_000006.12:33127425:T:TCT
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TCT=0./0 (ALFA)
TC=0.00028/4 (TOMMO)
HGVS:: NC_000006.12:g.33127426_33127427insCT, NC_000006.11:g.33095203_33095204insCT, NT_167244.2:g.4432048_4432049dup, NT_167244.1:g.4381964_4381965dup

Select item 14909538953.

rs1490953895 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:33115382 (GRCh38)
6:33083159 (GRCh37)
Canonical SPDI:: NC_000006.12:33115381:A:G
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.33115382A>G, NC_000006.11:g.33083159A>G, NT_113891.3:g.4527153A>G, NT_113891.2:g.4527259A>G, NT_167248.2:g.4310019A>G, NT_167248.1:g.4315615A>G, NT_167249.2:g.4564339A>G, NT_167249.1:g.4563637A>G, NT_167246.2:g.4535088A>G, NT_167246.1:g.4540708A>G, NT_167247.2:g.4414391A>G, NT_167247.1:g.4419976A>G, NT_167244.2:g.4420006A>G, NT_167244.1:g.4369922A>G

Select item 14901592434.

rs1490159243 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:33118193 (GRCh38)
6:33085970 (GRCh37)
Canonical SPDI:: NC_000006.12:33118192:C:T
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
T=0.000071/1 (TOMMO)
HGVS:: NC_000006.12:g.33118193C>T, NC_000006.11:g.33085970C>T, NT_113891.3:g.4529973C>T, NT_113891.2:g.4530079C>T, NT_167248.2:g.4312866C>T, NT_167248.1:g.4318462C>T, NT_167249.2:g.4567159C>T, NT_167249.1:g.4566457C>T, NT_167246.2:g.4537935C>T, NT_167246.1:g.4543555C>T, NT_167244.2:g.4422817C>T, NT_167244.1:g.4372733C>T

Select item 14897572725.

rs1489757272 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:33119718 (GRCh38)
6:33087495 (GRCh37)
Canonical SPDI:: NC_000006.12:33119717:T:C
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.33119718T>C, NC_000006.11:g.33087495T>C, NT_113891.3:g.4531499T>C, NT_113891.2:g.4531605T>C, NT_167248.2:g.4314392T>C, NT_167248.1:g.4319988T>C, NT_167249.2:g.4568685T>C, NT_167249.1:g.4567983T>C, NT_167246.2:g.4539461T>C, NT_167246.1:g.4545081T>C, NT_167244.2:g.4424342T>C, NT_167244.1:g.4374258T>C

Select item 14895174696.

rs1489517469 [Homo sapiens]

Variant type:: DELINS
Alleles:: AGTA>- [Show Flanks]
Chromosome:: 6:33111258 (GRCh38)
6:33079035 (GRCh37)
Canonical SPDI:: NC_000006.12:33111254:GTAAGTA:GTA
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: GTA=0./0 (ALFA)
-=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.33111258_33111261del, NC_000006.11:g.33079035_33079038del, NT_113891.3:g.4523029_4523032del, NT_113891.2:g.4523135_4523138del, NT_167248.2:g.4305894_4305897del, NT_167248.1:g.4311490_4311493del, NT_167249.2:g.4560215_4560218del, NT_167249.1:g.4559513_4559516del, NT_167246.2:g.4530963_4530966del, NT_167246.1:g.4536583_4536586del, NT_167247.2:g.4410268_4410271del, NT_167247.1:g.4415853_4415856del, NT_167244.2:g.4415883_4415886del, NT_167244.1:g.4365799_4365802del

Select item 14892047827.

rs1489204782 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 6:33119068 (GRCh38)
6:33086845 (GRCh37)
Canonical SPDI:: NC_000006.12:33119067:A:C,NC_000006.12:33119067:A:G
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
A=0.5/2 (SGDP_PRJ)
HGVS:: NC_000006.12:g.33119068A>C, NC_000006.12:g.33119068A>G, NC_000006.11:g.33086845A>C, NC_000006.11:g.33086845A>G, NT_113891.3:g.4530849A>C, NT_113891.3:g.4530849A>G, NT_113891.2:g.4530955A>C, NT_113891.2:g.4530955A>G, NT_167248.2:g.4313742A>C, NT_167248.2:g.4313742A>G, NT_167248.1:g.4319338A>C, NT_167248.1:g.4319338A>G, NT_167249.2:g.4568035A>C, NT_167249.2:g.4568035A>G, NT_167249.1:g.4567333A>C, NT_167249.1:g.4567333A>G, NT_167246.2:g.4538811A>C, NT_167246.2:g.4538811A>G, NT_167246.1:g.4544431A>C, NT_167246.1:g.4544431A>G, NT_167244.2:g.4423692A>C, NT_167244.2:g.4423692A>G, NT_167244.1:g.4373608A>C, NT_167244.1:g.4373608A>G

Select item 14888323688.

rs1488832368 [Homo sapiens]

Variant type:: DELINS
Alleles:: C>- [Show Flanks]
Chromosome:: 6:33128274 (GRCh38)
6:33096051 (GRCh37)
Canonical SPDI:: NC_000006.12:33128273:CCCCC:CCCC
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: CCCC=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.33128278del, NC_000006.11:g.33096055del, NT_113891.3:g.4539737del, NT_113891.2:g.4539843del, NT_167248.2:g.4322629del, NT_167248.1:g.4328225del, NT_167245.2:g.4371776del, NT_167245.1:g.4377361del, NT_167249.2:g.4576922del, NT_167249.1:g.4576220del, NT_167246.2:g.4547698del, NT_167246.1:g.4553318del, NT_167244.2:g.4432899del, NT_167244.1:g.4382815del, XR_007068748.1:n.6451del

Select item 14887301329.

rs1488730132 has merged into rs9280336 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTTTTTTT>-,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 6:33127433 (GRCh38)
6:33095210 (GRCh37)
Canonical SPDI:: NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:33127424:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTT=0./0 (ALFA)
TTTTTTTTTTTTTTTT=0./0 (GENOME_DK)
HGVS:: NC_000006.12:g.33127433_33127452del, NC_000006.12:g.33127436_33127452del, NC_000006.12:g.33127437_33127452del, NC_000006.12:g.33127438_33127452del, NC_000006.12:g.33127439_33127452del, NC_000006.12:g.33127440_33127452del, NC_000006.12:g.33127441_33127452del, NC_000006.12:g.33127442_33127452del, NC_000006.12:g.33127443_33127452del, NC_000006.12:g.33127444_33127452del, NC_000006.12:g.33127445_33127452del, NC_000006.12:g.33127446_33127452del, NC_000006.12:g.33127447_33127452del, NC_000006.12:g.33127448_33127452del, NC_000006.12:g.33127449_33127452del, NC_000006.12:g.33127450_33127452del, NC_000006.12:g.33127451_33127452del, NC_000006.12:g.33127452del, NC_000006.12:g.33127452dup, NC_000006.12:g.33127451_33127452dup, NC_000006.12:g.33127450_33127452dup, NC_000006.12:g.33127449_33127452dup, NC_000006.12:g.33127448_33127452dup, NC_000006.12:g.33127447_33127452dup, NC_000006.12:g.33127446_33127452dup, NC_000006.12:g.33127445_33127452dup, NC_000006.12:g.33127444_33127452dup, NC_000006.12:g.33127443_33127452dup, NC_000006.12:g.33127442_33127452dup, NC_000006.12:g.33127441_33127452dup, NC_000006.12:g.33127440_33127452dup, NC_000006.12:g.33127435_33127452dup, NC_000006.12:g.33127430_33127452dup, NC_000006.12:g.33127427_33127452dup, NC_000006.12:g.33127452_33127453insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.33127452_33127453insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.33127452_33127453insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.33095210_33095229del, NC_000006.11:g.33095213_33095229del, NC_000006.11:g.33095214_33095229del, NC_000006.11:g.33095215_33095229del, NC_000006.11:g.33095216_33095229del, NC_000006.11:g.33095217_33095229del, NC_000006.11:g.33095218_33095229del, NC_000006.11:g.33095219_33095229del, NC_000006.11:g.33095220_33095229del, NC_000006.11:g.33095221_33095229del, NC_000006.11:g.33095222_33095229del, NC_000006.11:g.33095223_33095229del, NC_000006.11:g.33095224_33095229del, NC_000006.11:g.33095225_33095229del, NC_000006.11:g.33095226_33095229del, NC_000006.11:g.33095227_33095229del, NC_000006.11:g.33095228_33095229del, NC_000006.11:g.33095229del, NC_000006.11:g.33095229dup, NC_000006.11:g.33095228_33095229dup, NC_000006.11:g.33095227_33095229dup, NC_000006.11:g.33095226_33095229dup, NC_000006.11:g.33095225_33095229dup, NC_000006.11:g.33095224_33095229dup, NC_000006.11:g.33095223_33095229dup, NC_000006.11:g.33095222_33095229dup, NC_000006.11:g.33095221_33095229dup, NC_000006.11:g.33095220_33095229dup, NC_000006.11:g.33095219_33095229dup, NC_000006.11:g.33095218_33095229dup, NC_000006.11:g.33095217_33095229dup, NC_000006.11:g.33095212_33095229dup, NC_000006.11:g.33095207_33095229dup, NC_000006.11:g.33095204_33095229dup, NC_000006.11:g.33095229_33095230insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.33095229_33095230insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.33095229_33095230insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.3:g.4538909_4538911dup, NT_113891.3:g.4538895_4538911del, NT_113891.3:g.4538898_4538911del, NT_113891.3:g.4538899_4538911del, NT_113891.3:g.4538900_4538911del, NT_113891.3:g.4538901_4538911del, NT_113891.3:g.4538902_4538911del, NT_113891.3:g.4538903_4538911del, NT_113891.3:g.4538904_4538911del, NT_113891.3:g.4538905_4538911del, NT_113891.3:g.4538906_4538911del, NT_113891.3:g.4538907_4538911del, NT_113891.3:g.4538908_4538911del, NT_113891.3:g.4538909_4538911del, NT_113891.3:g.4538910_4538911del, NT_113891.3:g.4538911del, NT_113891.3:g.4538911dup, NT_113891.3:g.4538910_4538911dup, NT_113891.3:g.4538908_4538911dup, NT_113891.3:g.4538907_4538911dup, NT_113891.3:g.4538906_4538911dup, NT_113891.3:g.4538905_4538911dup, NT_113891.3:g.4538904_4538911dup, NT_113891.3:g.4538903_4538911dup, NT_113891.3:g.4538902_4538911dup, NT_113891.3:g.4538901_4538911dup, NT_113891.3:g.4538900_4538911dup, NT_113891.3:g.4538899_4538911dup, NT_113891.3:g.4538898_4538911dup, NT_113891.3:g.4538897_4538911dup, NT_113891.3:g.4538896_4538911dup, NT_113891.3:g.4538891_4538911dup, NT_113891.3:g.4538911_4538912insTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.3:g.4538911_4538912insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.3:g.4538911_4538912insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.3:g.4538911_4538912insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.3:g.4538911_4538912insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.4321790_4321803dup, NT_167248.2:g.4321798_4321803del, NT_167248.2:g.4321801_4321803del, NT_167248.2:g.4321802_4321803del, NT_167248.2:g.4321803del, NT_167248.2:g.4321803dup, NT_167248.2:g.4321802_4321803dup, NT_167248.2:g.4321801_4321803dup, NT_167248.2:g.4321800_4321803dup, NT_167248.2:g.4321799_4321803dup, NT_167248.2:g.4321798_4321803dup, NT_167248.2:g.4321797_4321803dup, NT_167248.2:g.4321796_4321803dup, NT_167248.2:g.4321795_4321803dup, NT_167248.2:g.4321794_4321803dup, NT_167248.2:g.4321793_4321803dup, NT_167248.2:g.4321792_4321803dup, NT_167248.2:g.4321791_4321803dup, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTT, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTTT, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTTTT, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTTTTT, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.2:g.4321803_4321804insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.2:g.4576092_4576096dup, NT_167249.2:g.4576082_4576096del, NT_167249.2:g.4576085_4576096del, NT_167249.2:g.4576086_4576096del, NT_167249.2:g.4576087_4576096del, NT_167249.2:g.4576088_4576096del, NT_167249.2:g.4576089_4576096del, NT_167249.2:g.4576090_4576096del, NT_167249.2:g.4576091_4576096del, NT_167249.2:g.4576092_4576096del, NT_167249.2:g.4576093_4576096del, NT_167249.2:g.4576094_4576096del, NT_167249.2:g.4576095_4576096del, NT_167249.2:g.4576096del, NT_167249.2:g.4576096dup, NT_167249.2:g.4576095_4576096dup, NT_167249.2:g.4576094_4576096dup, NT_167249.2:g.4576093_4576096dup, NT_167249.2:g.4576091_4576096dup, NT_167249.2:g.4576090_4576096dup, NT_167249.2:g.4576089_4576096dup, NT_167249.2:g.4576088_4576096dup, NT_167249.2:g.4576087_4576096dup, NT_167249.2:g.4576086_4576096dup, NT_167249.2:g.4576085_4576096dup, NT_167249.2:g.4576084_4576096dup, NT_167249.2:g.4576083_4576096dup, NT_167249.2:g.4576082_4576096dup, NT_167249.2:g.4576081_4576096dup, NT_167249.2:g.4576080_4576096dup, NT_167249.2:g.4576079_4576096dup, NT_167249.2:g.4576074_4576096dup, NT_167249.2:g.4576096_4576097insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.2:g.4576096_4576097insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.2:g.4576096_4576097insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.2:g.4576096_4576097insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.2:g.4576096_4576097insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.4546859_4546872dup, NT_167246.2:g.4546867_4546872del, NT_167246.2:g.4546870_4546872del, NT_167246.2:g.4546871_4546872del, NT_167246.2:g.4546872del, NT_167246.2:g.4546872dup, NT_167246.2:g.4546871_4546872dup, NT_167246.2:g.4546870_4546872dup, NT_167246.2:g.4546869_4546872dup, NT_167246.2:g.4546868_4546872dup, NT_167246.2:g.4546867_4546872dup, NT_167246.2:g.4546866_4546872dup, NT_167246.2:g.4546865_4546872dup, NT_167246.2:g.4546864_4546872dup, NT_167246.2:g.4546863_4546872dup, NT_167246.2:g.4546862_4546872dup, NT_167246.2:g.4546861_4546872dup, NT_167246.2:g.4546860_4546872dup, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTT, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTTT, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTTTT, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTTTTT, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.2:g.4546872_4546873insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167244.2:g.4432048C>T, NT_167244.2:g.4432048_4432067del, NT_167244.2:g.4432048_4432064del, NT_167244.2:g.4432048_4432063del, NT_167244.2:g.4432048_4432062del, NT_167244.2:g.4432048_4432061del, NT_167244.2:g.4432048_4432060del, NT_167244.2:g.4432048_4432059del, NT_167244.2:g.4432048_4432058del, NT_167244.2:g.4432048_4432057del, NT_167244.2:g.4432048_4432056del, NT_167244.2:g.4432048_4432055del, NT_167244.2:g.4432048_4432054del, NT_167244.2:g.4432048_4432053del, NT_167244.2:g.4432048_4432052del, NT_167244.2:g.4432048_4432051del, NT_167244.2:g.4432045CTT[1], NT_167244.2:g.4432048_4432049del, NT_167244.2:g.4432048del, NT_167244.2:g.4432048delinsTT, NT_167244.2:g.4432048delinsTTT, NT_167244.2:g.4432048delinsTTTT, NT_167244.2:g.4432048delinsTTTTT, NT_167244.2:g.4432048delinsTTTTTT, NT_167244.2:g.4432048delinsTTTTTTT, NT_167244.2:g.4432048delinsTTTTTTTT, NT_167244.2:g.4432048delinsTTTTTTTTT, NT_167244.2:g.4432048delinsTTTTTTTTTT, NT_167244.2:g.4432048delinsTTTTTTTTTTT, NT_167244.2:g.4432048delinsTTTTTTTTTTTT, NT_167244.2:g.4432048delinsTTTTTTTTTTTTT, NT_167244.2:g.4432048delinsTTTTTTTTTTTTTT, NT_167244.2:g.4432048delinsTTTTTTTTTTTTTTTTTTT, NT_167244.2:g.4432048delinsTTTTTTTTTTTTTTTTTTTTTTTT, NT_167244.2:g.4432048delinsTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167244.2:g.4432048delinsTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167244.2:g.4432048delinsTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167244.2:g.4432048delinsTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167244.1:g.4381964C>T, NT_167244.1:g.4381964_4381983del, NT_167244.1:g.4381964_4381980del, NT_167244.1:g.4381964_4381979del, NT_167244.1:g.4381964_4381978del, NT_167244.1:g.4381964_4381977del, NT_167244.1:g.4381964_4381976del, NT_167244.1:g.4381964_4381975del, NT_167244.1:g.4381964_4381974del, NT_167244.1:g.4381964_4381973del, NT_167244.1:g.4381964_4381972del, NT_167244.1:g.4381964_4381971del, NT_167244.1:g.4381964_4381970del, NT_167244.1:g.4381964_4381969del, NT_167244.1:g.4381964_4381968del, NT_167244.1:g.4381964_4381967del, NT_167244.1:g.4381961CTT[1], NT_167244.1:g.4381964_4381965del, NT_167244.1:g.4381964del, NT_167244.1:g.4381964delinsTT, NT_167244.1:g.4381964delinsTTT, NT_167244.1:g.4381964delinsTTTT, NT_167244.1:g.4381964delinsTTTTT, NT_167244.1:g.4381964delinsTTTTTT, NT_167244.1:g.4381964delinsTTTTTTT, NT_167244.1:g.4381964delinsTTTTTTTT, NT_167244.1:g.4381964delinsTTTTTTTTT, NT_167244.1:g.4381964delinsTTTTTTTTTT, NT_167244.1:g.4381964delinsTTTTTTTTTTT, NT_167244.1:g.4381964delinsTTTTTTTTTTTT, NT_167244.1:g.4381964delinsTTTTTTTTTTTTT, NT_167244.1:g.4381964delinsTTTTTTTTTTTTTT, NT_167244.1:g.4381964delinsTTTTTTTTTTTTTTTTTTT, NT_167244.1:g.4381964delinsTTTTTTTTTTTTTTTTTTTTTTTT, NT_167244.1:g.4381964delinsTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167244.1:g.4381964delinsTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167244.1:g.4381964delinsTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167244.1:g.4381964delinsTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.2:g.4539015_4539017dup, NT_113891.2:g.4539001_4539017del, NT_113891.2:g.4539004_4539017del, NT_113891.2:g.4539005_4539017del, NT_113891.2:g.4539006_4539017del, NT_113891.2:g.4539007_4539017del, NT_113891.2:g.4539008_4539017del, NT_113891.2:g.4539009_4539017del, NT_113891.2:g.4539010_4539017del, NT_113891.2:g.4539011_4539017del, NT_113891.2:g.4539012_4539017del, NT_113891.2:g.4539013_4539017del, NT_113891.2:g.4539014_4539017del, NT_113891.2:g.4539015_4539017del, NT_113891.2:g.4539016_4539017del, NT_113891.2:g.4539017del, NT_113891.2:g.4539017dup, NT_113891.2:g.4539016_4539017dup, NT_113891.2:g.4539014_4539017dup, NT_113891.2:g.4539013_4539017dup, NT_113891.2:g.4539012_4539017dup, NT_113891.2:g.4539011_4539017dup, NT_113891.2:g.4539010_4539017dup, NT_113891.2:g.4539009_4539017dup, NT_113891.2:g.4539008_4539017dup, NT_113891.2:g.4539007_4539017dup, NT_113891.2:g.4539006_4539017dup, NT_113891.2:g.4539005_4539017dup, NT_113891.2:g.4539004_4539017dup, NT_113891.2:g.4539003_4539017dup, NT_113891.2:g.4539002_4539017dup, NT_113891.2:g.4538997_4539017dup, NT_113891.2:g.4539017_4539018insTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.2:g.4539017_4539018insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.2:g.4539017_4539018insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.2:g.4539017_4539018insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_113891.2:g.4539017_4539018insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.4327386_4327399dup, NT_167248.1:g.4327394_4327399del, NT_167248.1:g.4327397_4327399del, NT_167248.1:g.4327398_4327399del, NT_167248.1:g.4327399del, NT_167248.1:g.4327399dup, NT_167248.1:g.4327398_4327399dup, NT_167248.1:g.4327397_4327399dup, NT_167248.1:g.4327396_4327399dup, NT_167248.1:g.4327395_4327399dup, NT_167248.1:g.4327394_4327399dup, NT_167248.1:g.4327393_4327399dup, NT_167248.1:g.4327392_4327399dup, NT_167248.1:g.4327391_4327399dup, NT_167248.1:g.4327390_4327399dup, NT_167248.1:g.4327389_4327399dup, NT_167248.1:g.4327388_4327399dup, NT_167248.1:g.4327387_4327399dup, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTT, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTTT, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTTTT, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTTTTT, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167248.1:g.4327399_4327400insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.1:g.4575390_4575394dup, NT_167249.1:g.4575380_4575394del, NT_167249.1:g.4575383_4575394del, NT_167249.1:g.4575384_4575394del, NT_167249.1:g.4575385_4575394del, NT_167249.1:g.4575386_4575394del, NT_167249.1:g.4575387_4575394del, NT_167249.1:g.4575388_4575394del, NT_167249.1:g.4575389_4575394del, NT_167249.1:g.4575390_4575394del, NT_167249.1:g.4575391_4575394del, NT_167249.1:g.4575392_4575394del, NT_167249.1:g.4575393_4575394del, NT_167249.1:g.4575394del, NT_167249.1:g.4575394dup, NT_167249.1:g.4575393_4575394dup, NT_167249.1:g.4575392_4575394dup, NT_167249.1:g.4575391_4575394dup, NT_167249.1:g.4575389_4575394dup, NT_167249.1:g.4575388_4575394dup, NT_167249.1:g.4575387_4575394dup, NT_167249.1:g.4575386_4575394dup, NT_167249.1:g.4575385_4575394dup, NT_167249.1:g.4575384_4575394dup, NT_167249.1:g.4575383_4575394dup, NT_167249.1:g.4575382_4575394dup, NT_167249.1:g.4575381_4575394dup, NT_167249.1:g.4575380_4575394dup, NT_167249.1:g.4575379_4575394dup, NT_167249.1:g.4575378_4575394dup, NT_167249.1:g.4575377_4575394dup, NT_167249.1:g.4575372_4575394dup, NT_167249.1:g.4575394_4575395insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.1:g.4575394_4575395insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.1:g.4575394_4575395insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.1:g.4575394_4575395insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167249.1:g.4575394_4575395insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.4552479_4552492dup, NT_167246.1:g.4552487_4552492del, NT_167246.1:g.4552490_4552492del, NT_167246.1:g.4552491_4552492del, NT_167246.1:g.4552492del, NT_167246.1:g.4552492dup, NT_167246.1:g.4552491_4552492dup, NT_167246.1:g.4552490_4552492dup, NT_167246.1:g.4552489_4552492dup, NT_167246.1:g.4552488_4552492dup, NT_167246.1:g.4552487_4552492dup, NT_167246.1:g.4552486_4552492dup, NT_167246.1:g.4552485_4552492dup, NT_167246.1:g.4552484_4552492dup, NT_167246.1:g.4552483_4552492dup, NT_167246.1:g.4552482_4552492dup, NT_167246.1:g.4552481_4552492dup, NT_167246.1:g.4552480_4552492dup, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTT, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTTT, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTTTT, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTTTTT, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167246.1:g.4552492_4552493insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 148868833210.

rs1488688332 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:33111842 (GRCh38)
6:33079619 (GRCh37)
Canonical SPDI:: NC_000006.12:33111841:T:C
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000006.12:g.33111842T>C, NC_000006.11:g.33079619T>C, NT_113891.3:g.4523613T>C, NT_113891.2:g.4523719T>C, NT_167248.2:g.4306478T>C, NT_167248.1:g.4312074T>C, NT_167249.2:g.4560799T>C, NT_167249.1:g.4560097T>C, NT_167246.2:g.4531547T>C, NT_167246.1:g.4537167T>C, NT_167247.2:g.4410852T>C, NT_167247.1:g.4416437T>C, NT_167244.2:g.4416467T>C, NT_167244.1:g.4366383T>C

Select item 148827527711.

rs1488275277 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:33122894 (GRCh38)
6:33090671 (GRCh37)
Canonical SPDI:: NC_000006.12:33122893:T:C
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.00003/8 (TOPMED)
C=0.000043/6 (GnomAD)
HGVS:: NC_000006.12:g.33122894T>C, NC_000006.11:g.33090671T>C, NT_113891.3:g.4534686T>C, NT_113891.2:g.4534792T>C, NT_167248.2:g.4317579T>C, NT_167248.1:g.4323175T>C, NT_167249.2:g.4571872T>C, NT_167249.1:g.4571170T>C, NT_167246.2:g.4542648T>C, NT_167246.1:g.4548268T>C, NT_167244.2:g.4427517T>C, NT_167244.1:g.4377433T>C

Select item 148771500412.

rs1487715004 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 6:33115969 (GRCh38)
6:33083746 (GRCh37)
Canonical SPDI:: NC_000006.12:33115968:C:G
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.33115969C>G, NC_000006.11:g.33083746C>G, NT_113891.3:g.4527740C>G, NT_113891.2:g.4527846C>G, NT_167248.2:g.4310621C>G, NT_167248.1:g.4316217C>G, NT_167249.2:g.4564926C>G, NT_167249.1:g.4564224C>G, NT_167246.2:g.4535690C>G, NT_167246.1:g.4541310C>G, NT_167247.2:g.4414978C>G, NT_167247.1:g.4420563C>G, NT_167244.2:g.4420593C>G, NT_167244.1:g.4370509C>G

Select item 148756462513.

rs1487564625 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:33119696 (GRCh38)
6:33087473 (GRCh37)
Canonical SPDI:: NC_000006.12:33119695:G:A
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.33119696G>A, NC_000006.11:g.33087473G>A, NT_113891.3:g.4531477G>A, NT_113891.2:g.4531583G>A, NT_167248.2:g.4314370G>A, NT_167248.1:g.4319966G>A, NT_167249.2:g.4568663G>A, NT_167249.1:g.4567961G>A, NT_167246.2:g.4539439G>A, NT_167246.1:g.4545059G>A, NT_167244.2:g.4424320G>A, NT_167244.1:g.4374236G>A

Select item 148755936114.

rs1487559361 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,G [Show Flanks]
Chromosome:: 6:33128111 (GRCh38)
6:33095888 (GRCh37)
Canonical SPDI:: NC_000006.12:33128110:T:A,NC_000006.12:33128110:T:G
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.33128111T>A, NC_000006.12:g.33128111T>G, NC_000006.11:g.33095888T>A, NC_000006.11:g.33095888T>G, NT_113891.3:g.4539570T>A, NT_113891.3:g.4539570T>G, NT_113891.2:g.4539676T>A, NT_113891.2:g.4539676T>G, NT_167248.2:g.4322462T>A, NT_167248.2:g.4322462T>G, NT_167248.1:g.4328058T>A, NT_167248.1:g.4328058T>G, NT_167245.2:g.4371609T>A, NT_167245.2:g.4371609T>G, NT_167245.1:g.4377194T>A, NT_167245.1:g.4377194T>G, NT_167249.2:g.4576755T>A, NT_167249.2:g.4576755T>G, NT_167249.1:g.4576053T>A, NT_167249.1:g.4576053T>G, NT_167246.2:g.4547531T>A, NT_167246.2:g.4547531T>G, NT_167246.1:g.4553151T>A, NT_167246.1:g.4553151T>G, NT_167244.2:g.4432732T>A, NT_167244.2:g.4432732T>G, NT_167244.1:g.4382648T>A, NT_167244.1:g.4382648T>G, XR_007068748.1:n.6614A>T, XR_007068748.1:n.6614A>C

Select item 148735636715.

rs1487356367 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:33125246 (GRCh38)
6:33093023 (GRCh37)
Canonical SPDI:: NC_000006.12:33125245:G:A
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000019/5 (TOPMED)
HGVS:: NC_000006.12:g.33125246G>A, NC_000006.11:g.33093023G>A, NT_113891.3:g.4537038G>A, NT_113891.2:g.4537144G>A, NT_167248.2:g.4319933G>A, NT_167248.1:g.4325529G>A, NT_167249.2:g.4574226G>A, NT_167249.1:g.4573524G>A, NT_167246.2:g.4545002G>A, NT_167246.1:g.4550622G>A, NT_167244.2:g.4429869G>A, NT_167244.1:g.4379785G>A

Select item 148703463916.

rs1487034639 [Homo sapiens]

Variant type:: DELINS
Alleles:: ACTG>- [Show Flanks]
Chromosome:: 6:33112239 (GRCh38)
6:33080016 (GRCh37)
Canonical SPDI:: NC_000006.12:33112235:CTGACTG:CTG
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CTG=0./0 (ALFA)
-=0.000007/1 (GnomAD)
-=0.000011/3 (TOPMED)
-=0.000312/2 (1000Genomes)
-=0.008953/150 (TOMMO)
HGVS:: NC_000006.12:g.33112239_33112242del, NC_000006.11:g.33080016_33080019del, NT_113891.3:g.4524010_4524013del, NT_113891.2:g.4524116_4524119del, NT_167248.2:g.4306875_4306878del, NT_167248.1:g.4312471_4312474del, NT_167249.2:g.4561196_4561199del, NT_167249.1:g.4560494_4560497del, NT_167246.2:g.4531944_4531947del, NT_167246.1:g.4537564_4537567del, NT_167247.2:g.4411249_4411252del, NT_167247.1:g.4416834_4416837del, NT_167244.2:g.4416864_4416867del, NT_167244.1:g.4366780_4366783del

Select item 148669969117.

rs1486699691 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:33125574 (GRCh38)
6:33093351 (GRCh37)
Canonical SPDI:: NC_000006.12:33125573:C:T
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.33125574C>T, NC_000006.11:g.33093351C>T, NT_113891.3:g.4537366C>T, NT_113891.2:g.4537472C>T, NT_167248.2:g.4320261C>T, NT_167248.1:g.4325857C>T, NT_167249.2:g.4574554C>T, NT_167249.1:g.4573852C>T, NT_167246.2:g.4545330C>T, NT_167246.1:g.4550950C>T, NT_167244.2:g.4430197C>T, NT_167244.1:g.4380113C>T

Select item 148660655018.

rs1486606550 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G [Show Flanks]
Chromosome:: 6:33117068 (GRCh38)
6:33084846 (GRCh37)
Canonical SPDI:: NC_000006.12:33117068:GGGGG:GGGGGG
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GGGGGG=0./0 (ALFA)
G=0.00031/2 (1000Genomes)
HGVS:: NC_000006.12:g.33117073dup, NC_000006.11:g.33084850dup, NT_113891.3:g.4528853dup, NT_113891.2:g.4528959dup, NT_167248.2:g.4311746dup, NT_167248.1:g.4317342dup, NT_167249.2:g.4566039dup, NT_167249.1:g.4565337dup, NT_167246.2:g.4536815dup, NT_167246.1:g.4542435dup, NT_167247.2:g.4416082dup, NT_167247.1:g.4421667dup, NT_167244.2:g.4421697dup, NT_167244.1:g.4371613dup, NR_001435.2:n.217dup, NR_001435.1:n.217dup

Select item 148659424019.

rs1486594240 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:33122709 (GRCh38)
6:33090486 (GRCh37)
Canonical SPDI:: NC_000006.12:33122708:A:G
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000006.12:g.33122709A>G, NC_000006.11:g.33090486A>G, NT_113891.3:g.4534501A>G, NT_113891.2:g.4534607A>G, NT_167248.2:g.4317394A>G, NT_167248.1:g.4322990A>G, NT_167249.2:g.4571687A>G, NT_167249.1:g.4570985A>G, NT_167246.2:g.4542463A>G, NT_167246.1:g.4548083A>G, NT_167244.2:g.4427332A>G, NT_167244.1:g.4377248A>G

Select item 148644328620.

rs1486443286 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:33129407 (GRCh38)
6:33097184 (GRCh37)
Canonical SPDI:: NC_000006.12:33129406:A:G
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.33129407A>G, NC_000006.11:g.33097184A>G, NT_113891.3:g.4540864A>G, NT_113891.2:g.4540970A>G, NT_167248.2:g.4323757A>G, NT_167248.1:g.4329353A>G, NT_167245.2:g.4372905A>G, NT_167245.1:g.4378490A>G, NT_167249.2:g.4578051A>G, NT_167249.1:g.4577349A>G, NT_167246.2:g.4548826A>G, NT_167246.1:g.4554446A>G, NT_167244.2:g.4434028A>G, NT_167244.1:g.4383944A>G, XR_951524.3:n.2523T>C, XR_951524.1:n.2089T>C, XR_007068748.1:n.5320T>C

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