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Select item 14915302521.

rs1491530252 has merged into rs59173874 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTT>-,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 4:57103669 (GRCh38)
4:57969835 (GRCh37)
Canonical SPDI:: NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: IGFBP7 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000004.12:g.57103669_57103676del, NC_000004.12:g.57103671_57103676del, NC_000004.12:g.57103672_57103676del, NC_000004.12:g.57103673_57103676del, NC_000004.12:g.57103674_57103676del, NC_000004.12:g.57103675_57103676del, NC_000004.12:g.57103676del, NC_000004.12:g.57103676dup, NC_000004.12:g.57103675_57103676dup, NC_000004.12:g.57103674_57103676dup, NC_000004.12:g.57103673_57103676dup, NC_000004.12:g.57103672_57103676dup, NC_000004.12:g.57103671_57103676dup, NC_000004.12:g.57103670_57103676dup, NC_000004.12:g.57103669_57103676dup, NC_000004.12:g.57103668_57103676dup, NC_000004.12:g.57103661_57103676T[25]CTTTTTTTTTTTTTTTTTTT[1], NC_000004.12:g.57103667_57103676dup, NC_000004.12:g.57103666_57103676dup, NC_000004.12:g.57103665_57103676dup, NC_000004.12:g.57103664_57103676dup, NC_000004.12:g.57103662_57103676dup, NC_000004.12:g.57103661_57103676dup, NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTT, NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTT, NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.57969835_57969842del, NC_000004.11:g.57969837_57969842del, NC_000004.11:g.57969838_57969842del, NC_000004.11:g.57969839_57969842del, NC_000004.11:g.57969840_57969842del, NC_000004.11:g.57969841_57969842del, NC_000004.11:g.57969842del, NC_000004.11:g.57969842dup, NC_000004.11:g.57969841_57969842dup, NC_000004.11:g.57969840_57969842dup, NC_000004.11:g.57969839_57969842dup, NC_000004.11:g.57969838_57969842dup, NC_000004.11:g.57969837_57969842dup, NC_000004.11:g.57969836_57969842dup, NC_000004.11:g.57969835_57969842dup, NC_000004.11:g.57969834_57969842dup, NC_000004.11:g.57969827_57969842T[25]CTTTTTTTTTTTTTTTTTTT[1], NC_000004.11:g.57969833_57969842dup, NC_000004.11:g.57969832_57969842dup, NC_000004.11:g.57969831_57969842dup, NC_000004.11:g.57969830_57969842dup, NC_000004.11:g.57969828_57969842dup, NC_000004.11:g.57969827_57969842dup, NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTT, NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTT, NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_031877.1:g.11718_11725del, NG_031877.1:g.11720_11725del, NG_031877.1:g.11721_11725del, NG_031877.1:g.11722_11725del, NG_031877.1:g.11723_11725del, NG_031877.1:g.11724_11725del, NG_031877.1:g.11725del, NG_031877.1:g.11725dup, NG_031877.1:g.11724_11725dup, NG_031877.1:g.11723_11725dup, NG_031877.1:g.11722_11725dup, NG_031877.1:g.11721_11725dup, NG_031877.1:g.11720_11725dup, NG_031877.1:g.11719_11725dup, NG_031877.1:g.11718_11725dup, NG_031877.1:g.11717_11725dup, NG_031877.1:g.11710_11725A[19]GAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_031877.1:g.11716_11725dup, NG_031877.1:g.11715_11725dup, NG_031877.1:g.11714_11725dup, NG_031877.1:g.11713_11725dup, NG_031877.1:g.11711_11725dup, NG_031877.1:g.11710_11725dup, NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAA, NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAA, NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAA, NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAA, NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAAA, NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAAAA, NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAAAAA, NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAAAAAA, NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAAAAAAA, NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 14915077172.

rs1491507717 [Homo sapiens]

Variant type:: DEL
Alleles:: GT>- [Show Flanks]
Chromosome:: 4:57066974 (GRCh38)
4:57933140 (GRCh37)
Canonical SPDI:: NC_000004.12:57066973:GT:
Gene:: IGFBP7 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000004.12:g.57066974_57066975del, NC_000004.11:g.57933140_57933141del, NG_031877.1:g.48411_48412del

Select item 14914307863.

rs1491430786 has merged into rs61431158 [Homo sapiens]

Variant type:: DELINS
Alleles:: TT>-,T,TTT,TTTT [Show Flanks]
Chromosome:: 4:57066986 (GRCh38)
4:57933152 (GRCh37)
Canonical SPDI:: NC_000004.12:57066974:TTTTTTTTTTTTT:TTTTTTTTTTT,NC_000004.12:57066974:TTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000004.12:57066974:TTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000004.12:57066974:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT
Gene:: IGFBP7 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTT=0./0 (ALFA)
-=0.11667/70 (NorthernSweden)
-=0.125/5 (GENOME_DK)
-=0.21366/1070 (1000Genomes)
HGVS:: NC_000004.12:g.57066986_57066987del, NC_000004.12:g.57066987del, NC_000004.12:g.57066987dup, NC_000004.12:g.57066986_57066987dup, NC_000004.11:g.57933152_57933153del, NC_000004.11:g.57933153del, NC_000004.11:g.57933153dup, NC_000004.11:g.57933152_57933153dup, NG_031877.1:g.48410_48411del, NG_031877.1:g.48411del, NG_031877.1:g.48411dup, NG_031877.1:g.48410_48411dup

Select item 14913862354.

rs1491386235 has merged into rs538065423 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAA>-,A,AA,AAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAAAAAA [Show Flanks]
Chromosome:: 4:57093511 (GRCh38)
4:57959677 (GRCh37)
Canonical SPDI:: NC_000004.12:57093499:AAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000004.12:57093499:AAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000004.12:57093499:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000004.12:57093499:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000004.12:57093499:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000004.12:57093499:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000004.12:57093499:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000004.12:57093499:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA
Gene:: IGFBP7 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAAAA=0./0 (ALFA)
-=0.125/5 (GENOME_DK)
HGVS:: NC_000004.12:g.57093511_57093514del, NC_000004.12:g.57093512_57093514del, NC_000004.12:g.57093513_57093514del, NC_000004.12:g.57093514del, NC_000004.12:g.57093514dup, NC_000004.12:g.57093513_57093514dup, NC_000004.12:g.57093512_57093514dup, NC_000004.12:g.57093507_57093514dup, NC_000004.11:g.57959677_57959680del, NC_000004.11:g.57959678_57959680del, NC_000004.11:g.57959679_57959680del, NC_000004.11:g.57959680del, NC_000004.11:g.57959680dup, NC_000004.11:g.57959679_57959680dup, NC_000004.11:g.57959678_57959680dup, NC_000004.11:g.57959673_57959680dup, NG_031877.1:g.21883_21886del, NG_031877.1:g.21884_21886del, NG_031877.1:g.21885_21886del, NG_031877.1:g.21886del, NG_031877.1:g.21886dup, NG_031877.1:g.21885_21886dup, NG_031877.1:g.21884_21886dup, NG_031877.1:g.21879_21886dup

Select item 14913055045.

rs1491305504 has merged into rs57704332 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTT>-,T,TT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 4:57084799 (GRCh38)
4:57950965 (GRCh37)
Canonical SPDI:: NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57084788:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: IGFBP7 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000004.12:g.57084799_57084808del, NC_000004.12:g.57084800_57084808del, NC_000004.12:g.57084801_57084808del, NC_000004.12:g.57084804_57084808del, NC_000004.12:g.57084805_57084808del, NC_000004.12:g.57084806_57084808del, NC_000004.12:g.57084807_57084808del, NC_000004.12:g.57084808del, NC_000004.12:g.57084808dup, NC_000004.12:g.57084807_57084808dup, NC_000004.12:g.57084806_57084808dup, NC_000004.12:g.57084805_57084808dup, NC_000004.12:g.57084804_57084808dup, NC_000004.12:g.57084803_57084808dup, NC_000004.12:g.57084802_57084808dup, NC_000004.12:g.57084801_57084808dup, NC_000004.12:g.57084800_57084808dup, NC_000004.12:g.57084799_57084808dup, NC_000004.12:g.57084798_57084808dup, NC_000004.12:g.57084797_57084808dup, NC_000004.12:g.57084796_57084808dup, NC_000004.12:g.57084795_57084808dup, NC_000004.12:g.57084794_57084808dup, NC_000004.12:g.57084793_57084808dup, NC_000004.12:g.57084792_57084808dup, NC_000004.12:g.57084791_57084808dup, NC_000004.12:g.57084790_57084808dup, NC_000004.12:g.57084808_57084809insTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.57084808_57084809insTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.57084808_57084809insTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.57084808_57084809insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.57084808_57084809insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.57084808_57084809insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.57084808_57084809insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.57084808_57084809insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.57084808_57084809insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.57084808_57084809insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.57084808_57084809insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.57084808_57084809insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.57084808_57084809insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.57084789_57084808T[55]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000004.12:g.57084808_57084809insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.57084808_57084809insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.57084808_57084809insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.57084808_57084809insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.57084808_57084809insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.57084808_57084809insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.57950965_57950974del, NC_000004.11:g.57950966_57950974del, NC_000004.11:g.57950967_57950974del, NC_000004.11:g.57950970_57950974del, NC_000004.11:g.57950971_57950974del, NC_000004.11:g.57950972_57950974del, NC_000004.11:g.57950973_57950974del, NC_000004.11:g.57950974del, NC_000004.11:g.57950974dup, NC_000004.11:g.57950973_57950974dup, NC_000004.11:g.57950972_57950974dup, NC_000004.11:g.57950971_57950974dup, NC_000004.11:g.57950970_57950974dup, NC_000004.11:g.57950969_57950974dup, NC_000004.11:g.57950968_57950974dup, NC_000004.11:g.57950967_57950974dup, NC_000004.11:g.57950966_57950974dup, NC_000004.11:g.57950965_57950974dup, NC_000004.11:g.57950964_57950974dup, NC_000004.11:g.57950963_57950974dup, NC_000004.11:g.57950962_57950974dup, NC_000004.11:g.57950961_57950974dup, NC_000004.11:g.57950960_57950974dup, NC_000004.11:g.57950959_57950974dup, NC_000004.11:g.57950958_57950974dup, NC_000004.11:g.57950957_57950974dup, NC_000004.11:g.57950956_57950974dup, NC_000004.11:g.57950974_57950975insTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.57950974_57950975insTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.57950974_57950975insTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.57950974_57950975insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.57950974_57950975insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.57950974_57950975insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.57950974_57950975insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.57950974_57950975insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.57950974_57950975insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.57950974_57950975insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.57950974_57950975insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.57950974_57950975insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.57950974_57950975insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.57950955_57950974T[55]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000004.11:g.57950974_57950975insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.57950974_57950975insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.57950974_57950975insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.57950974_57950975insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.57950974_57950975insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.57950974_57950975insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_031877.1:g.30588_30597del, NG_031877.1:g.30589_30597del, NG_031877.1:g.30590_30597del, NG_031877.1:g.30593_30597del, NG_031877.1:g.30594_30597del, NG_031877.1:g.30595_30597del, NG_031877.1:g.30596_30597del, NG_031877.1:g.30597del, NG_031877.1:g.30597dup, NG_031877.1:g.30596_30597dup, NG_031877.1:g.30595_30597dup, NG_031877.1:g.30594_30597dup, NG_031877.1:g.30593_30597dup, NG_031877.1:g.30592_30597dup, NG_031877.1:g.30591_30597dup, NG_031877.1:g.30590_30597dup, NG_031877.1:g.30589_30597dup, NG_031877.1:g.30588_30597dup, NG_031877.1:g.30587_30597dup, NG_031877.1:g.30586_30597dup, NG_031877.1:g.30585_30597dup, NG_031877.1:g.30584_30597dup, NG_031877.1:g.30583_30597dup, NG_031877.1:g.30582_30597dup, NG_031877.1:g.30581_30597dup, NG_031877.1:g.30580_30597dup, NG_031877.1:g.30579_30597dup, NG_031877.1:g.30597_30598insAAAAAAAAAAAAAAAAAAAAA, NG_031877.1:g.30597_30598insAAAAAAAAAAAAAAAAAAAAAA, NG_031877.1:g.30597_30598insAAAAAAAAAAAAAAAAAAAAAAA, NG_031877.1:g.30597_30598insAAAAAAAAAAAAAAAAAAAAAAAA, NG_031877.1:g.30597_30598insAAAAAAAAAAAAAAAAAAAAAAAAA, NG_031877.1:g.30597_30598insAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_031877.1:g.30597_30598insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_031877.1:g.30597_30598insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_031877.1:g.30597_30598insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_031877.1:g.30597_30598insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_031877.1:g.30597_30598insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_031877.1:g.30597_30598insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_031877.1:g.30597_30598insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_031877.1:g.30578_30597A[30]TAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_031877.1:g.30597_30598insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_031877.1:g.30597_30598insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_031877.1:g.30597_30598insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_031877.1:g.30597_30598insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_031877.1:g.30597_30598insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_031877.1:g.30597_30598insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 14912919856.

rs1491291985 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>- [Show Flanks]
Chromosome:: 4:57088137 (GRCh38)
4:57954303 (GRCh37)
Canonical SPDI:: NC_000004.12:57088135:TCT:T
Gene:: IGFBP7 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
-=0.00004/1 (TOMMO)
HGVS:: NC_000004.12:g.57088137_57088138del, NC_000004.11:g.57954303_57954304del, NG_031877.1:g.27249_27250del

Select item 14912577957.

rs1491257795 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 4:57073593 (GRCh38)
4:57939759 (GRCh37)
Canonical SPDI:: NC_000004.12:57073592:CA:
Gene:: IGFBP7 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
HGVS:: NC_000004.12:g.57073593_57073594del, NC_000004.11:g.57939759_57939760del, NG_031877.1:g.41792_41793del

Select item 14912477398.

rs1491247739 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 4:57039065 (GRCh38)
4:57905231 (GRCh37)
Canonical SPDI:: NC_000004.12:57039064:CA:
Gene:: IGFBP7 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00051/6 (ALFA)
HGVS:: NC_000004.12:g.57039065_57039066del, NC_000004.11:g.57905231_57905232del, NG_031877.1:g.76320_76321del

Select item 14912268429.

rs1491226842 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 4:57091389 (GRCh38)
4:57957555 (GRCh37)
Canonical SPDI:: NC_000004.12:57091388:AT:
Gene:: IGFBP7 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000125/33 (TOPMED)
-=0.000128/18 (GnomAD)
-=0.000248/4 (TOMMO)
-=0.000312/2 (1000Genomes)
HGVS:: NC_000004.12:g.57091389_57091390del, NC_000004.11:g.57957555_57957556del, NG_031877.1:g.23996_23997del

Select item 149121683810.

rs1491216838 has merged into rs34976333 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTT>-,T,TT,TTTT,TTTTT,TTTTTT [Show Flanks]
Chromosome:: 4:57068889 (GRCh38)
4:57935055 (GRCh37)
Canonical SPDI:: NC_000004.12:57068881:TTTTTTTTTT:TTTTTTT,NC_000004.12:57068881:TTTTTTTTTT:TTTTTTTT,NC_000004.12:57068881:TTTTTTTTTT:TTTTTTTTT,NC_000004.12:57068881:TTTTTTTTTT:TTTTTTTTTTT,NC_000004.12:57068881:TTTTTTTTTT:TTTTTTTTTTTT,NC_000004.12:57068881:TTTTTTTTTT:TTTTTTTTTTTTT
Gene:: IGFBP7 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTT=0./0 (ALFA)
-=0.1872/747 (1000Genomes)
HGVS:: NC_000004.12:g.57068889_57068891del, NC_000004.12:g.57068890_57068891del, NC_000004.12:g.57068891del, NC_000004.12:g.57068891dup, NC_000004.12:g.57068890_57068891dup, NC_000004.12:g.57068889_57068891dup, NC_000004.11:g.57935055_57935057del, NC_000004.11:g.57935056_57935057del, NC_000004.11:g.57935057del, NC_000004.11:g.57935057dup, NC_000004.11:g.57935056_57935057dup, NC_000004.11:g.57935055_57935057dup, NG_031877.1:g.46502_46504del, NG_031877.1:g.46503_46504del, NG_031877.1:g.46504del, NG_031877.1:g.46504dup, NG_031877.1:g.46503_46504dup, NG_031877.1:g.46502_46504dup

Select item 149119934111.

rs1491199341 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GT [Show Flanks]
Chromosome:: 4:57084789 (GRCh38)
4:57950956 (GRCh37)
Canonical SPDI:: NC_000004.12:57084789:T:TGT
Gene:: IGFBP7 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by cluster
MAF:: TG=0.00018/3 (TOMMO)
HGVS:: NC_000004.12:g.57084790_57084791insGT, NC_000004.11:g.57950956_57950957insGT, NG_031877.1:g.30596_30597insCA

Select item 149119088612.

rs1491190886 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CTT [Show Flanks]
Chromosome:: 4:57103661 (GRCh38)
4:57969828 (GRCh37)
Canonical SPDI:: NC_000004.12:57103661:TT:TTCTT
Gene:: IGFBP7 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTCTT=0.0011/13 (ALFA)
TTC=0.0625/112 (GnomAD)
HGVS:: NC_000004.12:g.57103663_57103664insCTT, NC_000004.11:g.57969829_57969830insCTT, NG_031877.1:g.11724_11725insGAA

Select item 149118856313.

rs1491188563 has merged into rs71208974 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 4:57039076 (GRCh38)
4:57905242 (GRCh37)
Canonical SPDI:: NC_000004.12:57039065:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000004.12:57039065:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000004.12:57039065:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000004.12:57039065:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000004.12:57039065:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000004.12:57039065:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000004.12:57039065:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000004.12:57039065:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000004.12:57039065:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000004.12:57039065:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000004.12:57039065:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000004.12:57039065:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:57039065:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:57039065:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:57039065:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:57039065:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:57039065:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:57039065:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:57039065:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:57039065:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:57039065:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:57039065:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:57039065:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:57039065:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:57039065:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:57039065:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:57039065:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:57039065:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:57039065:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:57039065:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:57039065:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: IGFBP7 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAA=0./0 (ALFA)
AAAAAAAAAA=0./0 (GENOME_DK)
AAAAAAAAAA=0.2945/1475 (1000Genomes)
HGVS:: NC_000004.12:g.57039076_57039088del, NC_000004.12:g.57039077_57039088del, NC_000004.12:g.57039078_57039088del, NC_000004.12:g.57039079_57039088del, NC_000004.12:g.57039080_57039088del, NC_000004.12:g.57039081_57039088del, NC_000004.12:g.57039082_57039088del, NC_000004.12:g.57039084_57039088del, NC_000004.12:g.57039085_57039088del, NC_000004.12:g.57039086_57039088del, NC_000004.12:g.57039087_57039088del, NC_000004.12:g.57039088del, NC_000004.12:g.57039088dup, NC_000004.12:g.57039087_57039088dup, NC_000004.12:g.57039086_57039088dup, NC_000004.12:g.57039085_57039088dup, NC_000004.12:g.57039084_57039088dup, NC_000004.12:g.57039083_57039088dup, NC_000004.12:g.57039082_57039088dup, NC_000004.12:g.57039081_57039088dup, NC_000004.12:g.57039080_57039088dup, NC_000004.12:g.57039079_57039088dup, NC_000004.12:g.57039078_57039088dup, NC_000004.12:g.57039077_57039088dup, NC_000004.12:g.57039076_57039088dup, NC_000004.12:g.57039075_57039088dup, NC_000004.12:g.57039074_57039088dup, NC_000004.12:g.57039072_57039088dup, NC_000004.12:g.57039088_57039089insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.12:g.57039088_57039089insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.12:g.57039066_57039088A[31]GAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000004.11:g.57905242_57905254del, NC_000004.11:g.57905243_57905254del, NC_000004.11:g.57905244_57905254del, NC_000004.11:g.57905245_57905254del, NC_000004.11:g.57905246_57905254del, NC_000004.11:g.57905247_57905254del, NC_000004.11:g.57905248_57905254del, NC_000004.11:g.57905250_57905254del, NC_000004.11:g.57905251_57905254del, NC_000004.11:g.57905252_57905254del, NC_000004.11:g.57905253_57905254del, NC_000004.11:g.57905254del, NC_000004.11:g.57905254dup, NC_000004.11:g.57905253_57905254dup, NC_000004.11:g.57905252_57905254dup, NC_000004.11:g.57905251_57905254dup, NC_000004.11:g.57905250_57905254dup, NC_000004.11:g.57905249_57905254dup, NC_000004.11:g.57905248_57905254dup, NC_000004.11:g.57905247_57905254dup, NC_000004.11:g.57905246_57905254dup, NC_000004.11:g.57905245_57905254dup, NC_000004.11:g.57905244_57905254dup, NC_000004.11:g.57905243_57905254dup, NC_000004.11:g.57905242_57905254dup, NC_000004.11:g.57905241_57905254dup, NC_000004.11:g.57905240_57905254dup, NC_000004.11:g.57905238_57905254dup, NC_000004.11:g.57905254_57905255insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.11:g.57905254_57905255insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.11:g.57905232_57905254A[31]GAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_031877.1:g.76308_76320del, NG_031877.1:g.76309_76320del, NG_031877.1:g.76310_76320del, NG_031877.1:g.76311_76320del, NG_031877.1:g.76312_76320del, NG_031877.1:g.76313_76320del, NG_031877.1:g.76314_76320del, NG_031877.1:g.76316_76320del, NG_031877.1:g.76317_76320del, NG_031877.1:g.76318_76320del, NG_031877.1:g.76319_76320del, NG_031877.1:g.76320del, NG_031877.1:g.76320dup, NG_031877.1:g.76319_76320dup, NG_031877.1:g.76318_76320dup, NG_031877.1:g.76317_76320dup, NG_031877.1:g.76316_76320dup, NG_031877.1:g.76315_76320dup, NG_031877.1:g.76314_76320dup, NG_031877.1:g.76313_76320dup, NG_031877.1:g.76312_76320dup, NG_031877.1:g.76311_76320dup, NG_031877.1:g.76310_76320dup, NG_031877.1:g.76309_76320dup, NG_031877.1:g.76308_76320dup, NG_031877.1:g.76307_76320dup, NG_031877.1:g.76306_76320dup, NG_031877.1:g.76304_76320dup, NG_031877.1:g.76320_76321insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_031877.1:g.76320_76321insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_031877.1:g.76298_76320T[26]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]

Select item 149105137814.

rs1491051378 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->A [Show Flanks]
Chromosome:: 4:57042185 (GRCh38)
4:57908352 (GRCh37)
Canonical SPDI:: NC_000004.12:57042185:A:AA
Gene:: IGFBP7 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: AA=0./0 (ALFA)
HGVS:: NC_000004.12:g.57042186dup, NC_000004.11:g.57908352dup, NG_031877.1:g.73200dup

Select item 149102846615.

rs1491028466 has merged into rs35304758 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAA>-,AA,AAAA,AAAAAA,AAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 4:57034061 (GRCh38)
4:57900227 (GRCh37)
Canonical SPDI:: NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000004.12:57034049:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: IGFBP7 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAA=0./0 (ALFA)
AA=0.4856/2432 (1000Genomes)
HGVS:: NC_000004.12:g.57034061_57034068del, NC_000004.12:g.57034063_57034068del, NC_000004.12:g.57034065_57034068del, NC_000004.12:g.57034067_57034068del, NC_000004.12:g.57034068del, NC_000004.12:g.57034068dup, NC_000004.12:g.57034067_57034068dup, NC_000004.12:g.57034066_57034068dup, NC_000004.12:g.57034065_57034068dup, NC_000004.12:g.57034064_57034068dup, NC_000004.12:g.57034063_57034068dup, NC_000004.12:g.57034062_57034068dup, NC_000004.12:g.57034061_57034068dup, NC_000004.12:g.57034059_57034068dup, NC_000004.12:g.57034056_57034068dup, NC_000004.12:g.57034068_57034069insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000004.11:g.57900227_57900234del, NC_000004.11:g.57900229_57900234del, NC_000004.11:g.57900231_57900234del, NC_000004.11:g.57900233_57900234del, NC_000004.11:g.57900234del, NC_000004.11:g.57900234dup, NC_000004.11:g.57900233_57900234dup, NC_000004.11:g.57900232_57900234dup, NC_000004.11:g.57900231_57900234dup, NC_000004.11:g.57900230_57900234dup, NC_000004.11:g.57900229_57900234dup, NC_000004.11:g.57900228_57900234dup, NC_000004.11:g.57900227_57900234dup, NC_000004.11:g.57900225_57900234dup, NC_000004.11:g.57900222_57900234dup, NC_000004.11:g.57900234_57900235insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_031877.1:g.81329_81336del, NG_031877.1:g.81331_81336del, NG_031877.1:g.81333_81336del, NG_031877.1:g.81335_81336del, NG_031877.1:g.81336del, NG_031877.1:g.81336dup, NG_031877.1:g.81335_81336dup, NG_031877.1:g.81334_81336dup, NG_031877.1:g.81333_81336dup, NG_031877.1:g.81332_81336dup, NG_031877.1:g.81331_81336dup, NG_031877.1:g.81330_81336dup, NG_031877.1:g.81329_81336dup, NG_031877.1:g.81327_81336dup, NG_031877.1:g.81324_81336dup, NG_031877.1:g.81336_81337insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 149101100716.

rs1491011007 has merged into rs60116761 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTT>-,T,TT,TTT,TTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 4:57053030 (GRCh38)
4:57919196 (GRCh37)
Canonical SPDI:: NC_000004.12:57053019:TTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000004.12:57053019:TTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000004.12:57053019:TTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000004.12:57053019:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000004.12:57053019:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000004.12:57053019:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000004.12:57053019:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000004.12:57053019:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000004.12:57053019:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000004.12:57053019:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000004.12:57053019:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57053019:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:57053019:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: IGFBP7 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTT=0./0 (ALFA)
-=0.1801/902 (1000Genomes)
HGVS:: NC_000004.12:g.57053030_57053034del, NC_000004.12:g.57053031_57053034del, NC_000004.12:g.57053032_57053034del, NC_000004.12:g.57053033_57053034del, NC_000004.12:g.57053034del, NC_000004.12:g.57053034dup, NC_000004.12:g.57053033_57053034dup, NC_000004.12:g.57053032_57053034dup, NC_000004.12:g.57053031_57053034dup, NC_000004.12:g.57053030_57053034dup, NC_000004.12:g.57053029_57053034dup, NC_000004.12:g.57053028_57053034dup, NC_000004.12:g.57053023_57053034dup, NC_000004.11:g.57919196_57919200del, NC_000004.11:g.57919197_57919200del, NC_000004.11:g.57919198_57919200del, NC_000004.11:g.57919199_57919200del, NC_000004.11:g.57919200del, NC_000004.11:g.57919200dup, NC_000004.11:g.57919199_57919200dup, NC_000004.11:g.57919198_57919200dup, NC_000004.11:g.57919197_57919200dup, NC_000004.11:g.57919196_57919200dup, NC_000004.11:g.57919195_57919200dup, NC_000004.11:g.57919194_57919200dup, NC_000004.11:g.57919189_57919200dup, NG_031877.1:g.62362_62366del, NG_031877.1:g.62363_62366del, NG_031877.1:g.62364_62366del, NG_031877.1:g.62365_62366del, NG_031877.1:g.62366del, NG_031877.1:g.62366dup, NG_031877.1:g.62365_62366dup, NG_031877.1:g.62364_62366dup, NG_031877.1:g.62363_62366dup, NG_031877.1:g.62362_62366dup, NG_031877.1:g.62361_62366dup, NG_031877.1:g.62360_62366dup, NG_031877.1:g.62355_62366dup

Select item 149097510717.

rs1490975107 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->ATTGTCTCAAA [Show Flanks]
Chromosome:: 4:57092301 (GRCh38)
4:57958468 (GRCh37)
Canonical SPDI:: NC_000004.12:57092301:AAA:AAAATTGTCTCAAA
Gene:: IGFBP7 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAATTGTCTCAAA=0./0 (ALFA)
AAAATTGTCTC=0.000004/1 (TOPMED)
AAAATTGTCTC=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.57092302_57092304A[4]TTGTCTCAAA[1], NC_000004.11:g.57958468_57958470A[4]TTGTCTCAAA[1], NG_031877.1:g.23084_23085insGAGACAATTTT

Select item 149096483418.

rs1490964834 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CAAATCTTAATAAAG [Show Flanks]
Chromosome:: 4:57034496 (GRCh38)
4:57900663 (GRCh37)
Canonical SPDI:: NC_000004.12:57034496:TAATAAAGCAAATCTTAATAAAG:TAATAAAGCAAATCTTAATAAAGCAAATCTTAATAAAG
Gene:: IGFBP7 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TAATAAAGCAAATCTTAATAAAGCAAATCTTAATAAAG=0./0 (ALFA)
TAATAAAGCAAATCT=0.000004/1 (TOPMED)
TAATAAAGCAAATCT=0.000014/2 (GnomAD)
HGVS:: NC_000004.12:g.57034505_57034519dup, NC_000004.11:g.57900671_57900685dup, NG_031877.1:g.80875_80889dup

Select item 149095713719.

rs1490957137 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 4:57036778 (GRCh38)
4:57902944 (GRCh37)
Canonical SPDI:: NC_000004.12:57036777:A:T
Gene:: IGFBP7 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.57036778A>T, NC_000004.11:g.57902944A>T, NG_031877.1:g.78608T>A

Select item 149092194120.

rs1490921941 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 4:57109450 (GRCh38)
4:57975616 (GRCh37)
Canonical SPDI:: NC_000004.12:57109449:T:A
Gene:: IGFBP7 (Varview), IGFBP7-AS1 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000125/33 (TOPMED)
A=0.000129/18 (GnomAD)
HGVS:: NC_000004.12:g.57109450T>A, NC_000004.11:g.57975616T>A, NG_031877.1:g.5936A>T

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