SNP Links for Gene (Select 5321) - SNP

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Select item 14915366161.

rs1491536616 [Homo sapiens]

Variant type:: INS
Alleles:: ->TTA [Show Flanks]
Chromosome:: 1:186868094 (GRCh38)
1:186837227 (GRCh37)
Canonical SPDI:: NC_000001.11:186868094::TTA
Gene:: PLA2G4A (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
HGVS:: NC_000001.11:g.186868094_186868095insTTA, NC_000001.10:g.186837226_186837227insTTA, NG_012203.2:g.44195_44196insTTA

Select item 14915286182.

rs1491528618 [Homo sapiens]

Variant type:: DELINS
Alleles:: TA>-,TATA [Show Flanks]
Chromosome:: 1:186857479 (GRCh38)
1:186826611 (GRCh37)
Canonical SPDI:: NC_000001.11:186857471:ATATATATA:ATATATA,NC_000001.11:186857471:ATATATATA:ATATATATATA
Gene:: PLA2G4A (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATATATATATA=0./0 (ALFA)
-=0.000008/1 (GnomAD)
-=0.000071/1 (TOMMO)
HGVS:: NC_000001.11:g.186857473TA[3], NC_000001.11:g.186857473TA[5], NC_000001.10:g.186826605TA[3], NC_000001.10:g.186826605TA[5], NG_012203.2:g.33574TA[3], NG_012203.2:g.33574TA[5]

Select item 14915002543.

rs1491500254 has merged into rs71571011 [Homo sapiens]

Variant type:: DELINS
Alleles:: TATATATATATATATATATA>-,TA,TATA,TATATA,TATATATA,TATATATATA,TATATATATATA,TATATATATATATA,TATATATATATATATA,TATATATATATATATATA,TATATATATATATATATATATA,TATATATATATATATATATATATA,TATATATATATATATATATATATATA,TATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA [Show Flanks]
Chromosome:: 1:186934445 (GRCh38)
1:186903577 (GRCh37)
Canonical SPDI:: NC_000001.11:186934443:ATATATATATATATATATATA:A,NC_000001.11:186934443:ATATATATATATATATATATA:ATA,NC_000001.11:186934443:ATATATATATATATATATATA:ATATA,NC_000001.11:186934443:ATATATATATATATATATATA:ATATATA,NC_000001.11:186934443:ATATATATATATATATATATA:ATATATATA,NC_000001.11:186934443:ATATATATATATATATATATA:ATATATATATA,NC_000001.11:186934443:ATATATATATATATATATATA:ATATATATATATA,NC_000001.11:186934443:ATATATATATATATATATATA:ATATATATATATATA,NC_000001.11:186934443:ATATATATATATATATATATA:ATATATATATATATATA,NC_000001.11:186934443:ATATATATATATATATATATA:ATATATATATATATATATA,NC_000001.11:186934443:ATATATATATATATATATATA:ATATATATATATATATATATATA,NC_000001.11:186934443:ATATATATATATATATATATA:ATATATATATATATATATATATATA,NC_000001.11:186934443:ATATATATATATATATATATA:ATATATATATATATATATATATATATA,NC_000001.11:186934443:ATATATATATATATATATATA:ATATATATATATATATATATATATATATA,NC_000001.11:186934443:ATATATATATATATATATATA:ATATATATATATATATATATATATATATATA,NC_000001.11:186934443:ATATATATATATATATATATA:ATATATATATATATATATATATATATATATATA,NC_000001.11:186934443:ATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATA,NC_000001.11:186934443:ATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATATA,NC_000001.11:186934443:ATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATA,NC_000001.11:186934443:ATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATATA,NC_000001.11:186934443:ATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATATATA,NC_000001.11:186934443:ATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATATATATA,NC_000001.11:186934443:ATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATATATATATA,NC_000001.11:186934443:ATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000001.11:186934443:ATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000001.11:186934443:ATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000001.11:186934443:ATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000001.11:186934443:ATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000001.11:186934443:ATATATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA
Gene:: PLA2G4A (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATATATATATA=0./0 (ALFA)
ATATATATAT=0.2/8 (GENOME_DK)
HGVS:: NC_000001.11:g.186934445_186934464del, NC_000001.11:g.186934445TA[1], NC_000001.11:g.186934445TA[2], NC_000001.11:g.186934445TA[3], NC_000001.11:g.186934445TA[4], NC_000001.11:g.186934445TA[5], NC_000001.11:g.186934445TA[6], NC_000001.11:g.186934445TA[7], NC_000001.11:g.186934445TA[8], NC_000001.11:g.186934445TA[9], NC_000001.11:g.186934445TA[11], NC_000001.11:g.186934445TA[12], NC_000001.11:g.186934445TA[13], NC_000001.11:g.186934445TA[14], NC_000001.11:g.186934445TA[15], NC_000001.11:g.186934445TA[16], NC_000001.11:g.186934445TA[17], NC_000001.11:g.186934445TA[18], NC_000001.11:g.186934445TA[19], NC_000001.11:g.186934445TA[20], NC_000001.11:g.186934445TA[21], NC_000001.11:g.186934445TA[22], NC_000001.11:g.186934445TA[23], NC_000001.11:g.186934445TA[24], NC_000001.11:g.186934445TA[25], NC_000001.11:g.186934445TA[26], NC_000001.11:g.186934445TA[27], NC_000001.11:g.186934445TA[28], NC_000001.11:g.186934445TA[30], NC_000001.10:g.186903577_186903596del, NC_000001.10:g.186903577TA[1], NC_000001.10:g.186903577TA[2], NC_000001.10:g.186903577TA[3], NC_000001.10:g.186903577TA[4], NC_000001.10:g.186903577TA[5], NC_000001.10:g.186903577TA[6], NC_000001.10:g.186903577TA[7], NC_000001.10:g.186903577TA[8], NC_000001.10:g.186903577TA[9], NC_000001.10:g.186903577TA[11], NC_000001.10:g.186903577TA[12], NC_000001.10:g.186903577TA[13], NC_000001.10:g.186903577TA[14], NC_000001.10:g.186903577TA[15], NC_000001.10:g.186903577TA[16], NC_000001.10:g.186903577TA[17], NC_000001.10:g.186903577TA[18], NC_000001.10:g.186903577TA[19], NC_000001.10:g.186903577TA[20], NC_000001.10:g.186903577TA[21], NC_000001.10:g.186903577TA[22], NC_000001.10:g.186903577TA[23], NC_000001.10:g.186903577TA[24], NC_000001.10:g.186903577TA[25], NC_000001.10:g.186903577TA[26], NC_000001.10:g.186903577TA[27], NC_000001.10:g.186903577TA[28], NC_000001.10:g.186903577TA[30], NG_012203.2:g.110546_110565del, NG_012203.2:g.110546TA[1], NG_012203.2:g.110546TA[2], NG_012203.2:g.110546TA[3], NG_012203.2:g.110546TA[4], NG_012203.2:g.110546TA[5], NG_012203.2:g.110546TA[6], NG_012203.2:g.110546TA[7], NG_012203.2:g.110546TA[8], NG_012203.2:g.110546TA[9], NG_012203.2:g.110546TA[11], NG_012203.2:g.110546TA[12], NG_012203.2:g.110546TA[13], NG_012203.2:g.110546TA[14], NG_012203.2:g.110546TA[15], NG_012203.2:g.110546TA[16], NG_012203.2:g.110546TA[17], NG_012203.2:g.110546TA[18], NG_012203.2:g.110546TA[19], NG_012203.2:g.110546TA[20], NG_012203.2:g.110546TA[21], NG_012203.2:g.110546TA[22], NG_012203.2:g.110546TA[23], NG_012203.2:g.110546TA[24], NG_012203.2:g.110546TA[25], NG_012203.2:g.110546TA[26], NG_012203.2:g.110546TA[27], NG_012203.2:g.110546TA[28], NG_012203.2:g.110546TA[30]

Select item 14914998704.

rs1491499870 [Homo sapiens]

Variant type:: DEL
Alleles:: TG>- [Show Flanks]
Chromosome:: 1:186889691 (GRCh38)
1:186858823 (GRCh37)
Canonical SPDI:: NC_000001.11:186889690:TG:
Gene:: PLA2G4A (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000023/6 (TOPMED)
HGVS:: NC_000001.11:g.186889691_186889692del, NC_000001.10:g.186858823_186858824del, NG_012203.2:g.65792_65793del

Select item 14914688165.

rs1491468816 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GCTTGCTTGCTTGCTTTCTT,GCTTGCTTGCTTTCTT,GCTTGCTTGCTTTCTTTCTT,GCTTGCTTTCTT,GCTTGCTTTCTTTCTT,GCTTGCTTTCTTTCTTTCTT,GCTTTCTT,GCTTTCTTTCTT,GCTTTCTTTCTTTCTT,GCTTTCTTTCTTTCTTTCTT,GCTTTCTTTTTCTT,GCTTTCTTTTTCTTTCTT,GCTTTCTTTTTCTTTCTTTCTT [Show Flanks]
Chromosome:: 1:186830957 (GRCh38)
1:186800090 (GRCh37)
Canonical SPDI:: NC_000001.11:186830957:CTT:CTTGCTTGCTTGCTTGCTTTCTT,NC_000001.11:186830957:CTT:CTTGCTTGCTTGCTTTCTT,NC_000001.11:186830957:CTT:CTTGCTTGCTTGCTTTCTTTCTT,NC_000001.11:186830957:CTT:CTTGCTTGCTTTCTT,NC_000001.11:186830957:CTT:CTTGCTTGCTTTCTTTCTT,NC_000001.11:186830957:CTT:CTTGCTTGCTTTCTTTCTTTCTT,NC_000001.11:186830957:CTT:CTTGCTTTCTT,NC_000001.11:186830957:CTT:CTTGCTTTCTTTCTT,NC_000001.11:186830957:CTT:CTTGCTTTCTTTCTTTCTT,NC_000001.11:186830957:CTT:CTTGCTTTCTTTCTTTCTTTCTT,NC_000001.11:186830957:CTT:CTTGCTTTCTTTTTCTT,NC_000001.11:186830957:CTT:CTTGCTTTCTTTTTCTTTCTT,NC_000001.11:186830957:CTT:CTTGCTTTCTTTTTCTTTCTTTCTT
Gene:: PLA2G4A (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CTTGCTTTCTT=0./0 (ALFA)
CTTGCTTGCTTT=0.00386/82 (TOMMO)
HGVS:: NC_000001.11:g.186830958_186830960CTTG[4]CTTTCTT[1], NC_000001.11:g.186830958_186830960CTTG[3]CTTTCTT[1], NC_000001.11:g.186830958_186830960CTTG[3]CTTT[2]CTT[1], NC_000001.11:g.186830958_186830960CTTG[2]CTTTCTT[1], NC_000001.11:g.186830958_186830960CTTG[2]CTTT[2]CTT[1], NC_000001.11:g.186830958_186830960CTTG[2]CTTT[3]CTT[1], NC_000001.11:g.186830960_186830961insGCTTTCTT, NC_000001.11:g.186830960_186830961insGCTTTCTTTCTT, NC_000001.11:g.186830960_186830961insGCTTTCTTTCTTTCTT, NC_000001.11:g.186830960_186830961insGCTTTCTTTCTTTCTTTCTT, NC_000001.11:g.186830960_186830961insGCTTTCTTTTTCTT, NC_000001.11:g.186830960_186830961insGCTTTCTTTTTCTTTCTT, NC_000001.11:g.186830960_186830961insGCTTTCTTTTTCTTTCTTTCTT, NC_000001.10:g.186800090_186800092CTTG[4]CTTTCTT[1], NC_000001.10:g.186800090_186800092CTTG[3]CTTTCTT[1], NC_000001.10:g.186800090_186800092CTTG[3]CTTT[2]CTT[1], NC_000001.10:g.186800090_186800092CTTG[2]CTTTCTT[1], NC_000001.10:g.186800090_186800092CTTG[2]CTTT[2]CTT[1], NC_000001.10:g.186800090_186800092CTTG[2]CTTT[3]CTT[1], NC_000001.10:g.186800092_186800093insGCTTTCTT, NC_000001.10:g.186800092_186800093insGCTTTCTTTCTT, NC_000001.10:g.186800092_186800093insGCTTTCTTTCTTTCTT, NC_000001.10:g.186800092_186800093insGCTTTCTTTCTTTCTTTCTT, NC_000001.10:g.186800092_186800093insGCTTTCTTTTTCTT, NC_000001.10:g.186800092_186800093insGCTTTCTTTTTCTTTCTT, NC_000001.10:g.186800092_186800093insGCTTTCTTTTTCTTTCTTTCTT, NG_012203.2:g.7059_7061CTTG[4]CTTTCTT[1], NG_012203.2:g.7059_7061CTTG[3]CTTTCTT[1], NG_012203.2:g.7059_7061CTTG[3]CTTT[2]CTT[1], NG_012203.2:g.7059_7061CTTG[2]CTTTCTT[1], NG_012203.2:g.7059_7061CTTG[2]CTTT[2]CTT[1], NG_012203.2:g.7059_7061CTTG[2]CTTT[3]CTT[1], NG_012203.2:g.7061_7062insGCTTTCTT, NG_012203.2:g.7061_7062insGCTTTCTTTCTT, NG_012203.2:g.7061_7062insGCTTTCTTTCTTTCTT, NG_012203.2:g.7061_7062insGCTTTCTTTCTTTCTTTCTT, NG_012203.2:g.7061_7062insGCTTTCTTTTTCTT, NG_012203.2:g.7061_7062insGCTTTCTTTTTCTTTCTT, NG_012203.2:g.7061_7062insGCTTTCTTTTTCTTTCTTTCTT

Select item 14914540286.

rs1491454028 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 1:186909660 (GRCh38)
1:186878792 (GRCh37)
Canonical SPDI:: NC_000001.11:186909659:CA:
Gene:: PLA2G4A (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.02074/246 (ALFA)
-=0.00262/74 (TOMMO)
HGVS:: NC_000001.11:g.186909660_186909661del, NC_000001.10:g.186878792_186878793del, NG_012203.2:g.85761_85762del

Select item 14914384627.

rs1491438462 [Homo sapiens]

Variant type:: DEL
Alleles:: TG>- [Show Flanks]
Chromosome:: 1:186868094 (GRCh38)
1:186837226 (GRCh37)
Canonical SPDI:: NC_000001.11:186868093:TG:
Gene:: PLA2G4A (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.0011/13 (ALFA)
-=0.00071/20 (TOMMO)
HGVS:: NC_000001.11:g.186868094_186868095del, NC_000001.10:g.186837226_186837227del, NG_012203.2:g.44195_44196del

Select item 14913852858.

rs1491385285 has merged into rs67757094 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTT>-,TTTT,TTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 1:186932302 (GRCh38)
1:186901434 (GRCh37)
Canonical SPDI:: NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTT,NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTT,NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:186932294:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: PLA2G4A (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0./0 (ALFA)
-=0.000023/6 (TOPMED)
-=0.359225/1799 (1000Genomes)
HGVS:: NC_000001.11:g.186932302_186932307del, NC_000001.11:g.186932306_186932307del, NC_000001.11:g.186932307del, NC_000001.11:g.186932307dup, NC_000001.11:g.186932306_186932307dup, NC_000001.11:g.186932305_186932307dup, NC_000001.11:g.186932304_186932307dup, NC_000001.11:g.186932303_186932307dup, NC_000001.11:g.186932302_186932307dup, NC_000001.11:g.186932301_186932307dup, NC_000001.11:g.186932300_186932307dup, NC_000001.11:g.186932299_186932307dup, NC_000001.11:g.186932298_186932307dup, NC_000001.11:g.186932297_186932307dup, NC_000001.11:g.186932296_186932307dup, NC_000001.11:g.186932295_186932307dup, NC_000001.11:g.186932307_186932308insTTTTTTTTTTTTTT, NC_000001.11:g.186932307_186932308insTTTTTTTTTTTTTTTTT, NC_000001.11:g.186932307_186932308insTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.186932307_186932308insTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.186932307_186932308insTTTTTTTTTTTTTTTTTTTTTT, NC_000001.11:g.186932307_186932308insTTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.186901434_186901439del, NC_000001.10:g.186901438_186901439del, NC_000001.10:g.186901439del, NC_000001.10:g.186901439dup, NC_000001.10:g.186901438_186901439dup, NC_000001.10:g.186901437_186901439dup, NC_000001.10:g.186901436_186901439dup, NC_000001.10:g.186901435_186901439dup, NC_000001.10:g.186901434_186901439dup, NC_000001.10:g.186901433_186901439dup, NC_000001.10:g.186901432_186901439dup, NC_000001.10:g.186901431_186901439dup, NC_000001.10:g.186901430_186901439dup, NC_000001.10:g.186901429_186901439dup, NC_000001.10:g.186901428_186901439dup, NC_000001.10:g.186901427_186901439dup, NC_000001.10:g.186901439_186901440insTTTTTTTTTTTTTT, NC_000001.10:g.186901439_186901440insTTTTTTTTTTTTTTTTT, NC_000001.10:g.186901439_186901440insTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.186901439_186901440insTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.186901439_186901440insTTTTTTTTTTTTTTTTTTTTTT, NC_000001.10:g.186901439_186901440insTTTTTTTTTTTTTTTTTTTTTTT, NG_012203.2:g.108403_108408del, NG_012203.2:g.108407_108408del, NG_012203.2:g.108408del, NG_012203.2:g.108408dup, NG_012203.2:g.108407_108408dup, NG_012203.2:g.108406_108408dup, NG_012203.2:g.108405_108408dup, NG_012203.2:g.108404_108408dup, NG_012203.2:g.108403_108408dup, NG_012203.2:g.108402_108408dup, NG_012203.2:g.108401_108408dup, NG_012203.2:g.108400_108408dup, NG_012203.2:g.108399_108408dup, NG_012203.2:g.108398_108408dup, NG_012203.2:g.108397_108408dup, NG_012203.2:g.108396_108408dup, NG_012203.2:g.108408_108409insTTTTTTTTTTTTTT, NG_012203.2:g.108408_108409insTTTTTTTTTTTTTTTTT, NG_012203.2:g.108408_108409insTTTTTTTTTTTTTTTTTTTT, NG_012203.2:g.108408_108409insTTTTTTTTTTTTTTTTTTTTT, NG_012203.2:g.108408_108409insTTTTTTTTTTTTTTTTTTTTTT, NG_012203.2:g.108408_108409insTTTTTTTTTTTTTTTTTTTTTTT

Select item 14913458739.

rs1491345873 has merged into rs1490608809 [Homo sapiens]

Variant type:: DELINS
Alleles:: TATA>-,TA,TATAAGTATACATATATATATACTTATGTATATATATA,TATATA,TATATATATA [Show Flanks]
Chromosome:: 1:186912737 (GRCh38)
1:186881869 (GRCh37)
Canonical SPDI:: NC_000001.11:186912731:ATATATATA:ATATA,NC_000001.11:186912731:ATATATATA:ATATATA,NC_000001.11:186912731:ATATATATA:ATATATATAAGTATACATATATATATACTTATGTATATATATA,NC_000001.11:186912731:ATATATATA:ATATATATATA,NC_000001.11:186912731:ATATATATA:ATATATATATATATA
Gene:: PLA2G4A (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATATATA=0./0 (ALFA)
ATATAT=0.000008/1 (GnomAD)
AT=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.186912733TA[2], NC_000001.11:g.186912733TA[3], NC_000001.11:g.186912732_186912740AT[4]AAGTATACATATATATATACTTATGTATATATATA[1], NC_000001.11:g.186912733TA[5], NC_000001.11:g.186912733TA[7], NC_000001.10:g.186881865TA[2], NC_000001.10:g.186881865TA[3], NC_000001.10:g.186881864_186881872AT[4]AAGTATACATATATATATACTTATGTATATATATA[1], NC_000001.10:g.186881865TA[5], NC_000001.10:g.186881865TA[7], NG_012203.2:g.88834TA[2], NG_012203.2:g.88834TA[3], NG_012203.2:g.88833_88841AT[4]AAGTATACATATATATATACTTATGTATATATATA[1], NG_012203.2:g.88834TA[5], NG_012203.2:g.88834TA[7]

Select item 149131612210.

rs1491316122 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>-,CTCT [Show Flanks]
Chromosome:: 1:186830998 (GRCh38)
1:186800130 (GRCh37)
Canonical SPDI:: NC_000001.11:186830996:TCT:T,NC_000001.11:186830996:TCT:TCTCT
Gene:: PLA2G4A (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TCTCT=0./0 (ALFA)
-=0.000031/4 (GnomAD)
-=0.000112/3 (TOMMO)
HGVS:: NC_000001.11:g.186830998_186830999del, NC_000001.11:g.186830998_186830999dup, NC_000001.10:g.186800130_186800131del, NC_000001.10:g.186800130_186800131dup, NG_012203.2:g.7099_7100del, NG_012203.2:g.7099_7100dup

Select item 149130181711.

rs1491301817 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TCTT,TCTTTCTT,TCTTTCTTTCTT,TCTTTCTTTCTTTCTT [Show Flanks]
Chromosome:: 1:186830953 (GRCh38)
1:186800086 (GRCh37)
Canonical SPDI:: NC_000001.11:186830953:CTT:CTTTCTT,NC_000001.11:186830953:CTT:CTTTCTTTCTT,NC_000001.11:186830953:CTT:CTTTCTTTCTTTCTT,NC_000001.11:186830953:CTT:CTTTCTTTCTTTCTTTCTT
Gene:: PLA2G4A (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CTTTCTTTCTT=0./0 (ALFA)
CTTT=0.00186/43 (TOMMO)
HGVS:: NC_000001.11:g.186830956_186830957insTCTT, NC_000001.11:g.186830956_186830957insTCTTTCTT, NC_000001.11:g.186830957TCTT[3], NC_000001.11:g.186830957TCTT[4], NC_000001.10:g.186800088_186800089insTCTT, NC_000001.10:g.186800088_186800089insTCTTTCTT, NC_000001.10:g.186800089TCTT[3], NC_000001.10:g.186800089TCTT[4], NG_012203.2:g.7057_7058insTCTT, NG_012203.2:g.7057_7058insTCTTTCTT, NG_012203.2:g.7058TCTT[3], NG_012203.2:g.7058TCTT[4]

Select item 149126135312.

rs1491261353 has merged into rs1491084388 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>-,CTCT [Show Flanks]
Chromosome:: 1:186830970 (GRCh38)
1:186800102 (GRCh37)
Canonical SPDI:: NC_000001.11:186830968:TCT:T,NC_000001.11:186830968:TCT:TCTCT
Gene:: PLA2G4A (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: TCTCT=0./0 (ALFA)
-=0.00002/2 (GnomAD)
HGVS:: NC_000001.11:g.186830970_186830971del, NC_000001.11:g.186830970_186830971dup, NC_000001.10:g.186800102_186800103del, NC_000001.10:g.186800102_186800103dup, NG_012203.2:g.7071_7072del, NG_012203.2:g.7071_7072dup

Select item 149125421813.

rs1491254218 [Homo sapiens]

Variant type:: INS
Alleles:: ->TT [Show Flanks]
Chromosome:: 1:186828696 (GRCh38)
1:186797829 (GRCh37)
Canonical SPDI:: NC_000001.11:186828696::TT
Gene:: PLA2G4A (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
HGVS:: NC_000001.11:g.186828696_186828697insTT, NC_000001.10:g.186797828_186797829insTT, NG_012203.2:g.4797_4798insTT

Select item 149125226214.

rs1491252262 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->C [Show Flanks]
Chromosome:: 1:186830969 (GRCh38)
1:186800102 (GRCh37)
Canonical SPDI:: NC_000001.11:186830969:C:CC
Gene:: PLA2G4A (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: CC=0./0 (ALFA)
HGVS:: NC_000001.11:g.186830970dup, NC_000001.10:g.186800102dup, NG_012203.2:g.7071dup

Select item 149123820715.

rs1491238207 has merged into rs1267826917 [Homo sapiens]

Variant type:: DELINS
Alleles:: AA>-,A,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 1:186837757 (GRCh38)
1:186806889 (GRCh37)
Canonical SPDI:: NC_000001.11:186837753:AAAAA:AAA,NC_000001.11:186837753:AAAAA:AAAA,NC_000001.11:186837753:AAAAA:AAAAAA,NC_000001.11:186837753:AAAAA:AAAAAAA,NC_000001.11:186837753:AAAAA:AAAAAAAA,NC_000001.11:186837753:AAAAA:AAAAAAAAA,NC_000001.11:186837753:AAAAA:AAAAAAAAAA,NC_000001.11:186837753:AAAAA:AAAAAAAAAAA,NC_000001.11:186837753:AAAAA:AAAAAAAAAAAA,NC_000001.11:186837753:AAAAA:AAAAAAAAAAAAA,NC_000001.11:186837753:AAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186837753:AAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: PLA2G4A (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAA=0./0 (ALFA)
HGVS:: NC_000001.11:g.186837757_186837758del, NC_000001.11:g.186837758del, NC_000001.11:g.186837758dup, NC_000001.11:g.186837757_186837758dup, NC_000001.11:g.186837756_186837758dup, NC_000001.11:g.186837755_186837758dup, NC_000001.11:g.186837754_186837758dup, NC_000001.11:g.186837758_186837759insAAAAAA, NC_000001.11:g.186837758_186837759insAAAAAAA, NC_000001.11:g.186837758_186837759insAAAAAAAA, NC_000001.11:g.186837758_186837759insAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.186837758_186837759insAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.186806889_186806890del, NC_000001.10:g.186806890del, NC_000001.10:g.186806890dup, NC_000001.10:g.186806889_186806890dup, NC_000001.10:g.186806888_186806890dup, NC_000001.10:g.186806887_186806890dup, NC_000001.10:g.186806886_186806890dup, NC_000001.10:g.186806890_186806891insAAAAAA, NC_000001.10:g.186806890_186806891insAAAAAAA, NC_000001.10:g.186806890_186806891insAAAAAAAA, NC_000001.10:g.186806890_186806891insAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.186806890_186806891insAAAAAAAAAAAAAAAAAAAAAAA, NG_012203.2:g.13858_13859del, NG_012203.2:g.13859del, NG_012203.2:g.13859dup, NG_012203.2:g.13858_13859dup, NG_012203.2:g.13857_13859dup, NG_012203.2:g.13856_13859dup, NG_012203.2:g.13855_13859dup, NG_012203.2:g.13859_13860insAAAAAA, NG_012203.2:g.13859_13860insAAAAAAA, NG_012203.2:g.13859_13860insAAAAAAAA, NG_012203.2:g.13859_13860insAAAAAAAAAAAAAAAAAAAAAA, NG_012203.2:g.13859_13860insAAAAAAAAAAAAAAAAAAAAAAA

Select item 149123611016.

rs1491236110 has merged into rs68042430 [Homo sapiens]

Variant type:: DELINS
Alleles:: ATAT>-,AT,ATATAT [Show Flanks]
Chromosome:: 1:186912792 (GRCh38)
1:186881924 (GRCh37)
Canonical SPDI:: NC_000001.11:186912784:TATATATATAT:TATATAT,NC_000001.11:186912784:TATATATATAT:TATATATAT,NC_000001.11:186912784:TATATATATAT:TATATATATATAT
Gene:: PLA2G4A (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TATATATATATAT=0./0 (ALFA)
-=0.115/69 (NorthernSweden)
-=0.23333/7 (GENOME_DK)
-=0.24896/4172 (TOMMO)
HGVS:: NC_000001.11:g.186912786AT[3], NC_000001.11:g.186912786AT[4], NC_000001.11:g.186912786AT[6], NC_000001.10:g.186881918AT[3], NC_000001.10:g.186881918AT[4], NC_000001.10:g.186881918AT[6], NG_012203.2:g.88887AT[3], NG_012203.2:g.88887AT[4], NG_012203.2:g.88887AT[6]

Select item 149122228617.

rs1491222286 [Homo sapiens]

Variant type:: DEL
Alleles:: GC>- [Show Flanks]
Chromosome:: 1:186830957 (GRCh38)
1:186800089 (GRCh37)
Canonical SPDI:: NC_000001.11:186830956:GC:
Gene:: PLA2G4A (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.0306/363 (ALFA)
-=0.00035/6 (TOMMO)
-=0.00093/56 (GnomAD)
HGVS:: NC_000001.11:g.186830957_186830958del, NC_000001.10:g.186800089_186800090del, NG_012203.2:g.7058_7059del

Select item 149120650818.

rs1491206508 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->ATAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 1:186830609 (GRCh38)
1:186799742 (GRCh37)
Canonical SPDI:: NC_000001.11:186830609:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAA
Gene:: PLA2G4A (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
HGVS:: NC_000001.11:g.186830610_186830632A[24]TAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000001.10:g.186799742_186799764A[24]TAAAAAAAAAAAAAAAAAAAAAAA[1], NG_012203.2:g.6711_6733A[24]TAAAAAAAAAAAAAAAAAAAAAAA[1]

Select item 149120445619.

rs1491204456 has merged into rs55745208 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 1:186830622 (GRCh38)
1:186799754 (GRCh37)
Canonical SPDI:: NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:186830608:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: PLA2G4A (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAA=0./0 (ALFA)
-=0.1258/630 (1000Genomes)
-=0.3421/13 (GENOME_DK)
HGVS:: NC_000001.11:g.186830622_186830632del, NC_000001.11:g.186830623_186830632del, NC_000001.11:g.186830624_186830632del, NC_000001.11:g.186830625_186830632del, NC_000001.11:g.186830626_186830632del, NC_000001.11:g.186830627_186830632del, NC_000001.11:g.186830628_186830632del, NC_000001.11:g.186830629_186830632del, NC_000001.11:g.186830630_186830632del, NC_000001.11:g.186830631_186830632del, NC_000001.11:g.186830632del, NC_000001.11:g.186830632dup, NC_000001.11:g.186830631_186830632dup, NC_000001.11:g.186830630_186830632dup, NC_000001.11:g.186830629_186830632dup, NC_000001.11:g.186830628_186830632dup, NC_000001.11:g.186830627_186830632dup, NC_000001.11:g.186830626_186830632dup, NC_000001.11:g.186830625_186830632dup, NC_000001.11:g.186830624_186830632dup, NC_000001.11:g.186830623_186830632dup, NC_000001.11:g.186830622_186830632dup, NC_000001.11:g.186830621_186830632dup, NC_000001.11:g.186830620_186830632dup, NC_000001.11:g.186830619_186830632dup, NC_000001.11:g.186830618_186830632dup, NC_000001.11:g.186830617_186830632dup, NC_000001.11:g.186830616_186830632dup, NC_000001.11:g.186830615_186830632dup, NC_000001.11:g.186830614_186830632dup, NC_000001.11:g.186830613_186830632dup, NC_000001.11:g.186830612_186830632dup, NC_000001.11:g.186830611_186830632dup, NC_000001.11:g.186830610_186830632dup, NC_000001.11:g.186830609_186830632dup, NC_000001.11:g.186830632_186830633insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.186830632_186830633insAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.186830632_186830633insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.186830632_186830633insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.186830632_186830633insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.186830632_186830633insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.186830632_186830633insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.186830632_186830633insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.186830632_186830633insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.186830632_186830633insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.186830632_186830633insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.186830632_186830633insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.186830632_186830633insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.186830632_186830633insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.186830632_186830633insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.186830632_186830633insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.186830632_186830633insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.186830632_186830633insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.186830632_186830633insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.186799754_186799764del, NC_000001.10:g.186799755_186799764del, NC_000001.10:g.186799756_186799764del, NC_000001.10:g.186799757_186799764del, NC_000001.10:g.186799758_186799764del, NC_000001.10:g.186799759_186799764del, NC_000001.10:g.186799760_186799764del, NC_000001.10:g.186799761_186799764del, NC_000001.10:g.186799762_186799764del, NC_000001.10:g.186799763_186799764del, NC_000001.10:g.186799764del, NC_000001.10:g.186799764dup, NC_000001.10:g.186799763_186799764dup, NC_000001.10:g.186799762_186799764dup, NC_000001.10:g.186799761_186799764dup, NC_000001.10:g.186799760_186799764dup, NC_000001.10:g.186799759_186799764dup, NC_000001.10:g.186799758_186799764dup, NC_000001.10:g.186799757_186799764dup, NC_000001.10:g.186799756_186799764dup, NC_000001.10:g.186799755_186799764dup, NC_000001.10:g.186799754_186799764dup, NC_000001.10:g.186799753_186799764dup, NC_000001.10:g.186799752_186799764dup, NC_000001.10:g.186799751_186799764dup, NC_000001.10:g.186799750_186799764dup, NC_000001.10:g.186799749_186799764dup, NC_000001.10:g.186799748_186799764dup, NC_000001.10:g.186799747_186799764dup, NC_000001.10:g.186799746_186799764dup, NC_000001.10:g.186799745_186799764dup, NC_000001.10:g.186799744_186799764dup, NC_000001.10:g.186799743_186799764dup, NC_000001.10:g.186799742_186799764dup, NC_000001.10:g.186799741_186799764dup, NC_000001.10:g.186799764_186799765insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.186799764_186799765insAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.186799764_186799765insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.186799764_186799765insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.186799764_186799765insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.186799764_186799765insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.186799764_186799765insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.186799764_186799765insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.186799764_186799765insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.186799764_186799765insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.186799764_186799765insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.186799764_186799765insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.186799764_186799765insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.186799764_186799765insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.186799764_186799765insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.186799764_186799765insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.186799764_186799765insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.186799764_186799765insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.186799764_186799765insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_012203.2:g.6723_6733del, NG_012203.2:g.6724_6733del, NG_012203.2:g.6725_6733del, NG_012203.2:g.6726_6733del, NG_012203.2:g.6727_6733del, NG_012203.2:g.6728_6733del, NG_012203.2:g.6729_6733del, NG_012203.2:g.6730_6733del, NG_012203.2:g.6731_6733del, NG_012203.2:g.6732_6733del, NG_012203.2:g.6733del, NG_012203.2:g.6733dup, NG_012203.2:g.6732_6733dup, NG_012203.2:g.6731_6733dup, NG_012203.2:g.6730_6733dup, NG_012203.2:g.6729_6733dup, NG_012203.2:g.6728_6733dup, NG_012203.2:g.6727_6733dup, NG_012203.2:g.6726_6733dup, NG_012203.2:g.6725_6733dup, NG_012203.2:g.6724_6733dup, NG_012203.2:g.6723_6733dup, NG_012203.2:g.6722_6733dup, NG_012203.2:g.6721_6733dup, NG_012203.2:g.6720_6733dup, NG_012203.2:g.6719_6733dup, NG_012203.2:g.6718_6733dup, NG_012203.2:g.6717_6733dup, NG_012203.2:g.6716_6733dup, NG_012203.2:g.6715_6733dup, NG_012203.2:g.6714_6733dup, NG_012203.2:g.6713_6733dup, NG_012203.2:g.6712_6733dup, NG_012203.2:g.6711_6733dup, NG_012203.2:g.6710_6733dup, NG_012203.2:g.6733_6734insAAAAAAAAAAAAAAAAAAAAAAAAA, NG_012203.2:g.6733_6734insAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_012203.2:g.6733_6734insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_012203.2:g.6733_6734insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_012203.2:g.6733_6734insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_012203.2:g.6733_6734insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_012203.2:g.6733_6734insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_012203.2:g.6733_6734insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_012203.2:g.6733_6734insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_012203.2:g.6733_6734insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_012203.2:g.6733_6734insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_012203.2:g.6733_6734insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_012203.2:g.6733_6734insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_012203.2:g.6733_6734insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_012203.2:g.6733_6734insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_012203.2:g.6733_6734insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_012203.2:g.6733_6734insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_012203.2:g.6733_6734insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_012203.2:g.6733_6734insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 149120372920.

rs1491203729 [Homo sapiens]

Variant type:: DEL
Alleles:: TT>- [Show Flanks]
Chromosome:: 1:186912784 (GRCh38)
1:186881916 (GRCh37)
Canonical SPDI:: NC_000001.11:186912783:TT:
Gene:: PLA2G4A (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.00004/4 (GnomAD)
HGVS:: NC_000001.11:g.186912784_186912785del, NC_000001.10:g.186881916_186881917del, NG_012203.2:g.88885_88886del

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