SNP Links for Gene (Select 2932) - SNP

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Select item 14915883121.

rs1491588312 has merged into rs1173737285 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 3:120082397 (GRCh38)
3:119801244 (GRCh37)
Canonical SPDI:: NC_000003.12:120082385:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000003.12:120082385:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000003.12:120082385:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000003.12:120082385:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000003.12:120082385:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000003.12:120082385:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000003.12:120082385:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000003.12:120082385:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000003.12:120082385:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000003.12:120082385:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000003.12:120082385:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000003.12:120082385:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:120082385:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:120082385:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:120082385:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:120082385:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:120082385:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:120082385:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:120082385:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:120082385:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:120082385:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:120082385:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:120082385:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:120082385:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:120082385:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:120082385:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:120082385:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:120082385:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:120082385:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:120082385:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:120082385:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:120082385:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:120082385:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:120082385:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:120082385:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: GSK3B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000003.12:g.120082397_120082414del, NC_000003.12:g.120082398_120082414del, NC_000003.12:g.120082399_120082414del, NC_000003.12:g.120082400_120082414del, NC_000003.12:g.120082401_120082414del, NC_000003.12:g.120082402_120082414del, NC_000003.12:g.120082403_120082414del, NC_000003.12:g.120082404_120082414del, NC_000003.12:g.120082405_120082414del, NC_000003.12:g.120082406_120082414del, NC_000003.12:g.120082407_120082414del, NC_000003.12:g.120082408_120082414del, NC_000003.12:g.120082409_120082414del, NC_000003.12:g.120082410_120082414del, NC_000003.12:g.120082411_120082414del, NC_000003.12:g.120082412_120082414del, NC_000003.12:g.120082413_120082414del, NC_000003.12:g.120082414del, NC_000003.12:g.120082414dup, NC_000003.12:g.120082413_120082414dup, NC_000003.12:g.120082412_120082414dup, NC_000003.12:g.120082411_120082414dup, NC_000003.12:g.120082410_120082414dup, NC_000003.12:g.120082409_120082414dup, NC_000003.12:g.120082408_120082414dup, NC_000003.12:g.120082407_120082414dup, NC_000003.12:g.120082406_120082414dup, NC_000003.12:g.120082405_120082414dup, NC_000003.12:g.120082404_120082414dup, NC_000003.12:g.120082403_120082414dup, NC_000003.12:g.120082402_120082414dup, NC_000003.12:g.120082399_120082414dup, NC_000003.12:g.120082397_120082414dup, NC_000003.12:g.120082414_120082415insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.120082414_120082415insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.119801244_119801261del, NC_000003.11:g.119801245_119801261del, NC_000003.11:g.119801246_119801261del, NC_000003.11:g.119801247_119801261del, NC_000003.11:g.119801248_119801261del, NC_000003.11:g.119801249_119801261del, NC_000003.11:g.119801250_119801261del, NC_000003.11:g.119801251_119801261del, NC_000003.11:g.119801252_119801261del, NC_000003.11:g.119801253_119801261del, NC_000003.11:g.119801254_119801261del, NC_000003.11:g.119801255_119801261del, NC_000003.11:g.119801256_119801261del, NC_000003.11:g.119801257_119801261del, NC_000003.11:g.119801258_119801261del, NC_000003.11:g.119801259_119801261del, NC_000003.11:g.119801260_119801261del, NC_000003.11:g.119801261del, NC_000003.11:g.119801261dup, NC_000003.11:g.119801260_119801261dup, NC_000003.11:g.119801259_119801261dup, NC_000003.11:g.119801258_119801261dup, NC_000003.11:g.119801257_119801261dup, NC_000003.11:g.119801256_119801261dup, NC_000003.11:g.119801255_119801261dup, NC_000003.11:g.119801254_119801261dup, NC_000003.11:g.119801253_119801261dup, NC_000003.11:g.119801252_119801261dup, NC_000003.11:g.119801251_119801261dup, NC_000003.11:g.119801250_119801261dup, NC_000003.11:g.119801249_119801261dup, NC_000003.11:g.119801246_119801261dup, NC_000003.11:g.119801244_119801261dup, NC_000003.11:g.119801261_119801262insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.119801261_119801262insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_012922.1:g.17015_17032del, NG_012922.1:g.17016_17032del, NG_012922.1:g.17017_17032del, NG_012922.1:g.17018_17032del, NG_012922.1:g.17019_17032del, NG_012922.1:g.17020_17032del, NG_012922.1:g.17021_17032del, NG_012922.1:g.17022_17032del, NG_012922.1:g.17023_17032del, NG_012922.1:g.17024_17032del, NG_012922.1:g.17025_17032del, NG_012922.1:g.17026_17032del, NG_012922.1:g.17027_17032del, NG_012922.1:g.17028_17032del, NG_012922.1:g.17029_17032del, NG_012922.1:g.17030_17032del, NG_012922.1:g.17031_17032del, NG_012922.1:g.17032del, NG_012922.1:g.17032dup, NG_012922.1:g.17031_17032dup, NG_012922.1:g.17030_17032dup, NG_012922.1:g.17029_17032dup, NG_012922.1:g.17028_17032dup, NG_012922.1:g.17027_17032dup, NG_012922.1:g.17026_17032dup, NG_012922.1:g.17025_17032dup, NG_012922.1:g.17024_17032dup, NG_012922.1:g.17023_17032dup, NG_012922.1:g.17022_17032dup, NG_012922.1:g.17021_17032dup, NG_012922.1:g.17020_17032dup, NG_012922.1:g.17017_17032dup, NG_012922.1:g.17015_17032dup, NG_012922.1:g.17032_17033insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_012922.1:g.17032_17033insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 14915840852.

rs1491584085 [Homo sapiens]

Variant type:: INS
Alleles:: ->T [Show Flanks]
Chromosome:: 3:120090231 (GRCh38)
3:119809079 (GRCh37)
Canonical SPDI:: NC_000003.12:120090231::T
Gene:: GSK3B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000029/1 (GnomAD)
HGVS:: NC_000003.12:g.120090231_120090232insT, NC_000003.11:g.119809078_119809079insT, NG_012922.1:g.9186_9187insA

Select item 14915754973.

rs1491575497 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 3:120015649 (GRCh38)
3:119734496 (GRCh37)
Canonical SPDI:: NC_000003.12:120015648:CA:
Gene:: GSK3B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000003.12:g.120015649_120015650del, NC_000003.11:g.119734496_119734497del, NG_012922.1:g.83768_83769del

Select item 14915498094.

rs1491549809 has merged into rs34550759 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTT>-,T,TT,TTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTTT [Show Flanks]
Chromosome:: 3:119936361 (GRCh38)
3:119655208 (GRCh37)
Canonical SPDI:: NC_000003.12:119936354:TTTTTTTTTT:TTTTTT,NC_000003.12:119936354:TTTTTTTTTT:TTTTTTT,NC_000003.12:119936354:TTTTTTTTTT:TTTTTTTT,NC_000003.12:119936354:TTTTTTTTTT:TTTTTTTTT,NC_000003.12:119936354:TTTTTTTTTT:TTTTTTTTTTT,NC_000003.12:119936354:TTTTTTTTTT:TTTTTTTTTTTT,NC_000003.12:119936354:TTTTTTTTTT:TTTTTTTTTTTTT,NC_000003.12:119936354:TTTTTTTTTT:TTTTTTTTTTTTTTT
Gene:: GSK3B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTT=0./0 (ALFA)
T=0.4429/2218 (1000Genomes)
HGVS:: NC_000003.12:g.119936361_119936364del, NC_000003.12:g.119936362_119936364del, NC_000003.12:g.119936363_119936364del, NC_000003.12:g.119936364del, NC_000003.12:g.119936364dup, NC_000003.12:g.119936363_119936364dup, NC_000003.12:g.119936362_119936364dup, NC_000003.12:g.119936360_119936364dup, NC_000003.11:g.119655208_119655211del, NC_000003.11:g.119655209_119655211del, NC_000003.11:g.119655210_119655211del, NC_000003.11:g.119655211del, NC_000003.11:g.119655211dup, NC_000003.11:g.119655210_119655211dup, NC_000003.11:g.119655209_119655211dup, NC_000003.11:g.119655207_119655211dup, NG_012922.1:g.163060_163063del, NG_012922.1:g.163061_163063del, NG_012922.1:g.163062_163063del, NG_012922.1:g.163063del, NG_012922.1:g.163063dup, NG_012922.1:g.163062_163063dup, NG_012922.1:g.163061_163063dup, NG_012922.1:g.163059_163063dup

Select item 14915334695.

rs1491533469 [Homo sapiens]

Variant type:: SNV:
Alleles:: TG>-
Chromosome:: no mapping
Canonical SPDI:

Select item 14915262936.

rs1491526293 has merged into rs927567102 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAA>-,A,AA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 3:119949803 (GRCh38)
3:119668650 (GRCh37)
Canonical SPDI:: NC_000003.12:119949793:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000003.12:119949793:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000003.12:119949793:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000003.12:119949793:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000003.12:119949793:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000003.12:119949793:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000003.12:119949793:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000003.12:119949793:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000003.12:119949793:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000003.12:119949793:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000003.12:119949793:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000003.12:119949793:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:119949793:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:119949793:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:119949793:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:119949793:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:119949793:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: GSK3B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000003.12:g.119949803_119949814del, NC_000003.12:g.119949804_119949814del, NC_000003.12:g.119949805_119949814del, NC_000003.12:g.119949807_119949814del, NC_000003.12:g.119949808_119949814del, NC_000003.12:g.119949809_119949814del, NC_000003.12:g.119949810_119949814del, NC_000003.12:g.119949811_119949814del, NC_000003.12:g.119949812_119949814del, NC_000003.12:g.119949813_119949814del, NC_000003.12:g.119949814del, NC_000003.12:g.119949814dup, NC_000003.12:g.119949813_119949814dup, NC_000003.12:g.119949812_119949814dup, NC_000003.12:g.119949811_119949814dup, NC_000003.12:g.119949810_119949814dup, NC_000003.12:g.119949809_119949814dup, NC_000003.11:g.119668650_119668661del, NC_000003.11:g.119668651_119668661del, NC_000003.11:g.119668652_119668661del, NC_000003.11:g.119668654_119668661del, NC_000003.11:g.119668655_119668661del, NC_000003.11:g.119668656_119668661del, NC_000003.11:g.119668657_119668661del, NC_000003.11:g.119668658_119668661del, NC_000003.11:g.119668659_119668661del, NC_000003.11:g.119668660_119668661del, NC_000003.11:g.119668661del, NC_000003.11:g.119668661dup, NC_000003.11:g.119668660_119668661dup, NC_000003.11:g.119668659_119668661dup, NC_000003.11:g.119668658_119668661dup, NC_000003.11:g.119668657_119668661dup, NC_000003.11:g.119668656_119668661dup, NG_012922.1:g.149613_149624del, NG_012922.1:g.149614_149624del, NG_012922.1:g.149615_149624del, NG_012922.1:g.149617_149624del, NG_012922.1:g.149618_149624del, NG_012922.1:g.149619_149624del, NG_012922.1:g.149620_149624del, NG_012922.1:g.149621_149624del, NG_012922.1:g.149622_149624del, NG_012922.1:g.149623_149624del, NG_012922.1:g.149624del, NG_012922.1:g.149624dup, NG_012922.1:g.149623_149624dup, NG_012922.1:g.149622_149624dup, NG_012922.1:g.149621_149624dup, NG_012922.1:g.149620_149624dup, NG_012922.1:g.149619_149624dup

Select item 14915259897.

rs1491525989 [Homo sapiens]

Variant type:: SNV:
Alleles:: ->A
Chromosome:: no mapping
Canonical SPDI:

Select item 14915201828.

rs1491520182 [Homo sapiens]

Variant type:: DELINS
Alleles:: TA>- [Show Flanks]
Chromosome:: 3:119862524 (GRCh38)
3:119581371 (GRCh37)
Canonical SPDI:: NC_000003.12:119862522:ATA:A
Gene:: GSK3B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0.00008/1 (ALFA)
HGVS:: NC_000003.12:g.119862524_119862525del, NC_000003.11:g.119581371_119581372del, NG_012922.1:g.236894_236895del

Select item 14915055849.

rs1491505584 [Homo sapiens]

Variant type:: DELINS
Alleles:: TT>- [Show Flanks]
Chromosome:: 3:119940110 (GRCh38)
3:119658957 (GRCh37)
Canonical SPDI:: NC_000003.12:119940108:TTT:T
Gene:: GSK3B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000084/1 (ALFA)
-=0.000071/1 (TOMMO)
-=0.000075/9 (GnomAD)
HGVS:: NC_000003.12:g.119940110_119940111del, NC_000003.11:g.119658957_119658958del, NG_012922.1:g.159308_159309del

Select item 149148583010.

rs1491485830 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GAA [Show Flanks]
Chromosome:: 3:120027378 (GRCh38)
3:119746226 (GRCh37)
Canonical SPDI:: NC_000003.12:120027378:GAA:GAAGAA
Gene:: GSK3B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: GAAGAA=0./0 (ALFA)
HGVS:: NC_000003.12:g.120027379_120027381dup, NC_000003.11:g.119746226_119746228dup, NG_012922.1:g.72037_72039dup

Select item 149146774911.

rs1491467749 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 3:119929901 (GRCh38)
3:119648748 (GRCh37)
Canonical SPDI:: NC_000003.12:119929900:CA:
Gene:: GSK3B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00008/1 (ALFA)
HGVS:: NC_000003.12:g.119929901_119929902del, NC_000003.11:g.119648748_119648749del, NG_012922.1:g.169516_169517del

Select item 149145624012.

rs1491456240 [Homo sapiens]

Variant type:: DEL
Alleles:: TA>- [Show Flanks]
Chromosome:: 3:119930080 (GRCh38)
3:119648927 (GRCh37)
Canonical SPDI:: NC_000003.12:119930079:TA:
Gene:: GSK3B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00008/1 (ALFA)
HGVS:: NC_000003.12:g.119930080_119930081del, NC_000003.11:g.119648927_119648928del, NG_012922.1:g.169337_169338del

Select item 149141604913.

rs1491416049 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TGTT [Show Flanks]
Chromosome:: 3:119822159 (GRCh38)
3:119541007 (GRCh37)
Canonical SPDI:: NC_000003.12:119822159:TGTT:TGTTTGTT
Gene:: GSK3B (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: TGTTTGTT=0./0 (ALFA)
TGTT=0.000014/2 (GnomAD)
HGVS:: NC_000003.12:g.119822160_119822163dup, NC_000003.11:g.119541007_119541010dup, NG_012922.1:g.277255_277258dup, NM_002093.4:c.*4625_*4628dup, NM_002093.3:c.*4625_*4628dup, NM_001146156.2:c.*4625_*4628dup, NM_001146156.1:c.*4625_*4628dup, NM_001354596.2:c.*4625_*4628dup, NM_001354596.1:c.*4625_*4628dup, XM_006713610.4:c.*4625_*4628dup, XM_006713610.3:c.*4625_*4628dup, XM_006713610.2:c.*4625_*4628dup, XM_006713610.1:c.*4625_*4628dup

Select item 149141522914.

rs1491415229 [Homo sapiens]

Variant type:: SNV:
Alleles:: GT>-
Chromosome:: no mapping
Canonical SPDI:

Select item 149139812715.

rs1491398127 [Homo sapiens]

Variant type:: DELINS
Alleles:: AG>- [Show Flanks]
Chromosome:: 3:119942349 (GRCh38)
3:119661196 (GRCh37)
Canonical SPDI:: NC_000003.12:119942347:GAG:G
Gene:: GSK3B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
-=0.000019/5 (TOPMED)
-=0.00005/7 (GnomAD)
HGVS:: NC_000003.12:g.119942349_119942350del, NC_000003.11:g.119661196_119661197del, NG_012922.1:g.157069_157070del

Select item 149139528116.

rs1491395281 [Homo sapiens]

Variant type:: INS
Alleles:: ->C,CAC,CTT [Show Flanks]
Chromosome:: 3:120079350 (GRCh38)
3:119798198 (GRCh37)
Canonical SPDI:: NC_000003.12:120079350::C,NC_000003.12:120079350::CAC,NC_000003.12:120079350::CTT
Gene:: GSK3B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CAC=0./0 (ALFA)
HGVS:: NC_000003.12:g.120079350_120079351insC, NC_000003.12:g.120079350_120079351insCAC, NC_000003.12:g.120079350_120079351insCTT, NC_000003.11:g.119798197_119798198insC, NC_000003.11:g.119798197_119798198insCAC, NC_000003.11:g.119798197_119798198insCTT, NG_012922.1:g.20067_20068insG, NG_012922.1:g.20067_20068insGTG, NG_012922.1:g.20067_20068insAAG

Select item 149138368317.

rs1491383683 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 3:120079350 (GRCh38)
3:119798197 (GRCh37)
Canonical SPDI:: NC_000003.12:120079349:AT:
Gene:: GSK3B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.00014/2 (TOMMO)
-=0.0002/18 (GnomAD)
HGVS:: NC_000003.12:g.120079350_120079351del, NC_000003.11:g.119798197_119798198del, NG_012922.1:g.20067_20068del

Select item 149138149018.

rs1491381490 has merged into rs779477802 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTT>-,T,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 3:119865475 (GRCh38)
3:119584322 (GRCh37)
Canonical SPDI:: NC_000003.12:119865466:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTT,NC_000003.12:119865466:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000003.12:119865466:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000003.12:119865466:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000003.12:119865466:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000003.12:119865466:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000003.12:119865466:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000003.12:119865466:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000003.12:119865466:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000003.12:119865466:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000003.12:119865466:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000003.12:119865466:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000003.12:119865466:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:119865466:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:119865466:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:119865466:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:119865466:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:119865466:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:119865466:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: GSK3B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTT=0./0 (ALFA)
TTTTTTTTT=0.325/13 (GENOME_DK)
HGVS:: NC_000003.12:g.119865475_119865489del, NC_000003.12:g.119865476_119865489del, NC_000003.12:g.119865479_119865489del, NC_000003.12:g.119865480_119865489del, NC_000003.12:g.119865481_119865489del, NC_000003.12:g.119865482_119865489del, NC_000003.12:g.119865483_119865489del, NC_000003.12:g.119865484_119865489del, NC_000003.12:g.119865485_119865489del, NC_000003.12:g.119865486_119865489del, NC_000003.12:g.119865487_119865489del, NC_000003.12:g.119865488_119865489del, NC_000003.12:g.119865489del, NC_000003.12:g.119865489dup, NC_000003.12:g.119865488_119865489dup, NC_000003.12:g.119865487_119865489dup, NC_000003.12:g.119865486_119865489dup, NC_000003.12:g.119865485_119865489dup, NC_000003.12:g.119865484_119865489dup, NC_000003.11:g.119584322_119584336del, NC_000003.11:g.119584323_119584336del, NC_000003.11:g.119584326_119584336del, NC_000003.11:g.119584327_119584336del, NC_000003.11:g.119584328_119584336del, NC_000003.11:g.119584329_119584336del, NC_000003.11:g.119584330_119584336del, NC_000003.11:g.119584331_119584336del, NC_000003.11:g.119584332_119584336del, NC_000003.11:g.119584333_119584336del, NC_000003.11:g.119584334_119584336del, NC_000003.11:g.119584335_119584336del, NC_000003.11:g.119584336del, NC_000003.11:g.119584336dup, NC_000003.11:g.119584335_119584336dup, NC_000003.11:g.119584334_119584336dup, NC_000003.11:g.119584333_119584336dup, NC_000003.11:g.119584332_119584336dup, NC_000003.11:g.119584331_119584336dup, NG_012922.1:g.233937_233951del, NG_012922.1:g.233938_233951del, NG_012922.1:g.233941_233951del, NG_012922.1:g.233942_233951del, NG_012922.1:g.233943_233951del, NG_012922.1:g.233944_233951del, NG_012922.1:g.233945_233951del, NG_012922.1:g.233946_233951del, NG_012922.1:g.233947_233951del, NG_012922.1:g.233948_233951del, NG_012922.1:g.233949_233951del, NG_012922.1:g.233950_233951del, NG_012922.1:g.233951del, NG_012922.1:g.233951dup, NG_012922.1:g.233950_233951dup, NG_012922.1:g.233949_233951dup, NG_012922.1:g.233948_233951dup, NG_012922.1:g.233947_233951dup, NG_012922.1:g.233946_233951dup

Select item 149137896019.

rs1491378960 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->A [Show Flanks]
Chromosome:: 3:119942348 (GRCh38)
3:119661196 (GRCh37)
Canonical SPDI:: NC_000003.12:119942348:A:AA
Gene:: GSK3B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AA=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.119942349dup, NC_000003.11:g.119661196dup, NG_012922.1:g.157069dup

Select item 149137665720.

rs1491376657 [Homo sapiens]

Variant type:: DEL
Alleles:: AA>- [Show Flanks]
Chromosome:: 3:119922271 (GRCh38)
3:119641118 (GRCh37)
Canonical SPDI:: NC_000003.12:119922270:AA:
Gene:: GSK3B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency
MAF:: -=0.000022/3 (GnomAD)
HGVS:: NC_000003.12:g.119922271_119922272del, NC_000003.11:g.119641118_119641119del, NG_012922.1:g.177146_177147del

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