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Select item 14914597561.

rs1491459756 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 11:60086857 (GRCh38)
11:59854330 (GRCh37)
Canonical SPDI:: NC_000011.10:60086856:CA:
Gene:: MS4A2 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0.00051/6 (ALFA)
HGVS:: NC_000011.10:g.60086857_60086858del, NC_000011.9:g.59854330_59854331del, NG_016014.1:g.3194_3195del, NW_019805498.1:g.180735_180736del

Select item 14911028382.

rs1491102838 has merged into rs34673841 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 11:60086867 (GRCh38)
11:59854340 (GRCh37)
Canonical SPDI:: NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:60086857:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: MS4A2 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAA=0./0 (ALFA)
AAAAAAAAAAAAAAAAA=0./0 (GENOME_DK)
HGVS:: NC_000011.10:g.60086867_60086884del, NC_000011.10:g.60086868_60086884del, NC_000011.10:g.60086869_60086884del, NC_000011.10:g.60086870_60086884del, NC_000011.10:g.60086871_60086884del, NC_000011.10:g.60086872_60086884del, NC_000011.10:g.60086873_60086884del, NC_000011.10:g.60086874_60086884del, NC_000011.10:g.60086875_60086884del, NC_000011.10:g.60086876_60086884del, NC_000011.10:g.60086877_60086884del, NC_000011.10:g.60086878_60086884del, NC_000011.10:g.60086879_60086884del, NC_000011.10:g.60086880_60086884del, NC_000011.10:g.60086881_60086884del, NC_000011.10:g.60086882_60086884del, NC_000011.10:g.60086883_60086884del, NC_000011.10:g.60086884del, NC_000011.10:g.60086884dup, NC_000011.10:g.60086883_60086884dup, NC_000011.10:g.60086882_60086884dup, NC_000011.10:g.60086881_60086884dup, NC_000011.10:g.60086880_60086884dup, NC_000011.10:g.60086879_60086884dup, NC_000011.10:g.60086878_60086884dup, NC_000011.10:g.60086877_60086884dup, NC_000011.10:g.60086876_60086884dup, NC_000011.10:g.60086875_60086884dup, NC_000011.10:g.60086874_60086884dup, NC_000011.10:g.60086873_60086884dup, NC_000011.10:g.60086872_60086884dup, NC_000011.10:g.60086871_60086884dup, NC_000011.10:g.60086870_60086884dup, NC_000011.10:g.60086869_60086884dup, NC_000011.10:g.60086868_60086884dup, NC_000011.10:g.60086867_60086884dup, NC_000011.10:g.60086866_60086884dup, NC_000011.10:g.60086865_60086884dup, NC_000011.10:g.60086864_60086884dup, NC_000011.10:g.60086863_60086884dup, NC_000011.10:g.60086860_60086884dup, NC_000011.10:g.60086859_60086884dup, NC_000011.10:g.60086858_60086884dup, NC_000011.10:g.60086884_60086885insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.60086884_60086885insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.60086884_60086885insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.60086884_60086885insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.10:g.60086858_60086884A[31]GAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000011.9:g.59854340_59854357del, NC_000011.9:g.59854341_59854357del, NC_000011.9:g.59854342_59854357del, NC_000011.9:g.59854343_59854357del, NC_000011.9:g.59854344_59854357del, NC_000011.9:g.59854345_59854357del, NC_000011.9:g.59854346_59854357del, NC_000011.9:g.59854347_59854357del, NC_000011.9:g.59854348_59854357del, NC_000011.9:g.59854349_59854357del, NC_000011.9:g.59854350_59854357del, NC_000011.9:g.59854351_59854357del, NC_000011.9:g.59854352_59854357del, NC_000011.9:g.59854353_59854357del, NC_000011.9:g.59854354_59854357del, NC_000011.9:g.59854355_59854357del, NC_000011.9:g.59854356_59854357del, NC_000011.9:g.59854357del, NC_000011.9:g.59854357dup, NC_000011.9:g.59854356_59854357dup, NC_000011.9:g.59854355_59854357dup, NC_000011.9:g.59854354_59854357dup, NC_000011.9:g.59854353_59854357dup, NC_000011.9:g.59854352_59854357dup, NC_000011.9:g.59854351_59854357dup, NC_000011.9:g.59854350_59854357dup, NC_000011.9:g.59854349_59854357dup, NC_000011.9:g.59854348_59854357dup, NC_000011.9:g.59854347_59854357dup, NC_000011.9:g.59854346_59854357dup, NC_000011.9:g.59854345_59854357dup, NC_000011.9:g.59854344_59854357dup, NC_000011.9:g.59854343_59854357dup, NC_000011.9:g.59854342_59854357dup, NC_000011.9:g.59854341_59854357dup, NC_000011.9:g.59854340_59854357dup, NC_000011.9:g.59854339_59854357dup, NC_000011.9:g.59854338_59854357dup, NC_000011.9:g.59854337_59854357dup, NC_000011.9:g.59854336_59854357dup, NC_000011.9:g.59854333_59854357dup, NC_000011.9:g.59854332_59854357dup, NC_000011.9:g.59854331_59854357dup, NC_000011.9:g.59854357_59854358insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.59854357_59854358insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.59854357_59854358insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.59854357_59854358insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000011.9:g.59854331_59854357A[31]GAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_016014.1:g.3204_3221del, NG_016014.1:g.3205_3221del, NG_016014.1:g.3206_3221del, NG_016014.1:g.3207_3221del, NG_016014.1:g.3208_3221del, NG_016014.1:g.3209_3221del, NG_016014.1:g.3210_3221del, NG_016014.1:g.3211_3221del, NG_016014.1:g.3212_3221del, NG_016014.1:g.3213_3221del, NG_016014.1:g.3214_3221del, NG_016014.1:g.3215_3221del, NG_016014.1:g.3216_3221del, NG_016014.1:g.3217_3221del, NG_016014.1:g.3218_3221del, NG_016014.1:g.3219_3221del, NG_016014.1:g.3220_3221del, NG_016014.1:g.3221del, NG_016014.1:g.3221dup, NG_016014.1:g.3220_3221dup, NG_016014.1:g.3219_3221dup, NG_016014.1:g.3218_3221dup, NG_016014.1:g.3217_3221dup, NG_016014.1:g.3216_3221dup, NG_016014.1:g.3215_3221dup, NG_016014.1:g.3214_3221dup, NG_016014.1:g.3213_3221dup, NG_016014.1:g.3212_3221dup, NG_016014.1:g.3211_3221dup, NG_016014.1:g.3210_3221dup, NG_016014.1:g.3209_3221dup, NG_016014.1:g.3208_3221dup, NG_016014.1:g.3207_3221dup, NG_016014.1:g.3206_3221dup, NG_016014.1:g.3205_3221dup, NG_016014.1:g.3204_3221dup, NG_016014.1:g.3203_3221dup, NG_016014.1:g.3202_3221dup, NG_016014.1:g.3201_3221dup, NG_016014.1:g.3200_3221dup, NG_016014.1:g.3197_3221dup, NG_016014.1:g.3196_3221dup, NG_016014.1:g.3195_3221dup, NG_016014.1:g.3221_3222insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_016014.1:g.3221_3222insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_016014.1:g.3221_3222insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_016014.1:g.3221_3222insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_016014.1:g.3195_3221A[31]GAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NW_019805498.1:g.180745_180762del, NW_019805498.1:g.180746_180762del, NW_019805498.1:g.180747_180762del, NW_019805498.1:g.180748_180762del, NW_019805498.1:g.180749_180762del, NW_019805498.1:g.180750_180762del, NW_019805498.1:g.180751_180762del, NW_019805498.1:g.180752_180762del, NW_019805498.1:g.180753_180762del, NW_019805498.1:g.180754_180762del, NW_019805498.1:g.180755_180762del, NW_019805498.1:g.180756_180762del, NW_019805498.1:g.180757_180762del, NW_019805498.1:g.180758_180762del, NW_019805498.1:g.180759_180762del, NW_019805498.1:g.180760_180762del, NW_019805498.1:g.180761_180762del, NW_019805498.1:g.180762del, NW_019805498.1:g.180762dup, NW_019805498.1:g.180761_180762dup, NW_019805498.1:g.180760_180762dup, NW_019805498.1:g.180759_180762dup, NW_019805498.1:g.180758_180762dup, NW_019805498.1:g.180757_180762dup, NW_019805498.1:g.180756_180762dup, NW_019805498.1:g.180755_180762dup, NW_019805498.1:g.180754_180762dup, NW_019805498.1:g.180753_180762dup, NW_019805498.1:g.180752_180762dup, NW_019805498.1:g.180751_180762dup, NW_019805498.1:g.180750_180762dup, NW_019805498.1:g.180749_180762dup, NW_019805498.1:g.180748_180762dup, NW_019805498.1:g.180747_180762dup, NW_019805498.1:g.180746_180762dup, NW_019805498.1:g.180745_180762dup, NW_019805498.1:g.180744_180762dup, NW_019805498.1:g.180743_180762dup, NW_019805498.1:g.180742_180762dup, NW_019805498.1:g.180741_180762dup, NW_019805498.1:g.180738_180762dup, NW_019805498.1:g.180737_180762dup, NW_019805498.1:g.180736_180762dup, NW_019805498.1:g.180762_180763insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NW_019805498.1:g.180762_180763insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NW_019805498.1:g.180762_180763insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NW_019805498.1:g.180762_180763insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NW_019805498.1:g.180736_180762A[31]GAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]

Select item 14910284823.

rs1491028482 has merged into rs3038646 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTT>-,T,TT,TTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTTT [Show Flanks]
Chromosome:: 11:60092310 (GRCh38)
11:59859783 (GRCh37)
Canonical SPDI:: NC_000011.10:60092296:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000011.10:60092296:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000011.10:60092296:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000011.10:60092296:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000011.10:60092296:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000011.10:60092296:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000011.10:60092296:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000011.10:60092296:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT
Gene:: MS4A2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTT=0./0 (ALFA)
TT=0.00667/4 (NorthernSweden)
-=0.11861/594 (1000Genomes)
HGVS:: NC_000011.10:g.60092310_60092313del, NC_000011.10:g.60092311_60092313del, NC_000011.10:g.60092312_60092313del, NC_000011.10:g.60092313del, NC_000011.10:g.60092313dup, NC_000011.10:g.60092312_60092313dup, NC_000011.10:g.60092311_60092313dup, NC_000011.10:g.60092309_60092313dup, NC_000011.9:g.59859783_59859786del, NC_000011.9:g.59859784_59859786del, NC_000011.9:g.59859785_59859786del, NC_000011.9:g.59859786del, NC_000011.9:g.59859786dup, NC_000011.9:g.59859785_59859786dup, NC_000011.9:g.59859784_59859786dup, NC_000011.9:g.59859782_59859786dup, NG_016014.1:g.8647_8650del, NG_016014.1:g.8648_8650del, NG_016014.1:g.8649_8650del, NG_016014.1:g.8650del, NG_016014.1:g.8650dup, NG_016014.1:g.8649_8650dup, NG_016014.1:g.8648_8650dup, NG_016014.1:g.8646_8650dup

Select item 14907922564.

rs1490792256 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 11:60095668 (GRCh38)
11:59863141 (GRCh37)
Canonical SPDI:: NC_000011.10:60095667:C:A,NC_000011.10:60095667:C:T
Gene:: MS4A2 (Varview)
Functional Consequence:: 3_prime_UTR_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000054/1 (ALFA)
A=0.000004/1 (TOPMED)
T=0.000223/1 (Estonian)
T=0.000546/1 (Korea1K)
HGVS:: NC_000011.10:g.60095668C>A, NC_000011.10:g.60095668C>T, NC_000011.9:g.59863141C>A, NC_000011.9:g.59863141C>T, NG_016014.1:g.12005C>A, NG_016014.1:g.12005C>T, NM_000139.5:c.*12C>A, NM_000139.5:c.*12C>T, NM_000139.4:c.*12C>A, NM_000139.4:c.*12C>T, NM_001256916.2:c.*12C>A, NM_001256916.2:c.*12C>T, NM_001256916.1:c.*12C>A, NM_001256916.1:c.*12C>T, XM_005273846.5:c.*12C>A, XM_005273846.5:c.*12C>T, XM_005273846.4:c.*12C>A, XM_005273846.4:c.*12C>T, XM_005273846.3:c.*12C>A, XM_005273846.3:c.*12C>T, XM_005273846.2:c.*12C>A, XM_005273846.2:c.*12C>T, XM_005273846.1:c.*12C>A, XM_005273846.1:c.*12C>T, XM_011544850.3:c.*12C>A, XM_011544850.3:c.*12C>T, XM_011544850.2:c.*12C>A, XM_011544850.2:c.*12C>T, XM_011544850.1:c.*12C>A, XM_011544850.1:c.*12C>T

Select item 14907724155.

rs1490772415 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:60098752 (GRCh38)
11:59866225 (GRCh37)
Canonical SPDI:: NC_000011.10:60098751:A:G
Gene:: MS4A2 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.60098752A>G, NC_000011.9:g.59866225A>G, NG_016014.1:g.15089A>G

Select item 14902943456.

rs1490294345 [Homo sapiens]

Variant type:: DEL
Alleles:: CAT>- [Show Flanks]
Chromosome:: 11:60088690 (GRCh38)
11:59856163 (GRCh37)
Canonical SPDI:: NC_000011.10:60088689:CAT:
Gene:: MS4A2 (Varview)
Functional Consequence:: 5_prime_UTR_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.60088690_60088692del, NC_000011.9:g.59856163_59856165del, NG_016014.1:g.5027_5029del, NM_000139.5:c.-76_-74del, NM_000139.4:c.-76_-74del, NM_001256916.2:c.-76_-74del, NM_001256916.1:c.-76_-74del, NM_001142303.1:c.-76_-74del

Select item 14902890787.

rs1490289078 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:60093644 (GRCh38)
11:59861117 (GRCh37)
Canonical SPDI:: NC_000011.10:60093643:A:G
Gene:: MS4A2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.60093644A>G, NC_000011.9:g.59861117A>G, NG_016014.1:g.9981A>G, NM_001142303.1:c.*35A>G

Select item 14902284078.

rs1490228407 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:60089946 (GRCh38)
11:59857419 (GRCh37)
Canonical SPDI:: NC_000011.10:60089945:G:C
Gene:: MS4A2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.60089946G>C, NC_000011.9:g.59857419G>C, NG_016014.1:g.6283G>C

Select item 14901852709.

rs1490185270 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 11:60095424 (GRCh38)
11:59862897 (GRCh37)
Canonical SPDI:: NC_000011.10:60095423:G:C,NC_000011.10:60095423:G:T
Gene:: MS4A2 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000011.10:g.60095424G>C, NC_000011.10:g.60095424G>T, NC_000011.9:g.59862897G>C, NC_000011.9:g.59862897G>T, NG_016014.1:g.11761G>C, NG_016014.1:g.11761G>T

Select item 149010829310.

rs1490108293 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 11:60097908 (GRCh38)
11:59865381 (GRCh37)
Canonical SPDI:: NC_000011.10:60097907:T:G
Gene:: MS4A2 (Varview)
Functional Consequence:: 3_prime_UTR_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.60097908T>G, NC_000011.9:g.59865381T>G, NG_016014.1:g.14245T>G, NM_000139.5:c.*2252T>G, NM_000139.4:c.*2252T>G, NM_001256916.2:c.*2252T>G, NM_001256916.1:c.*2252T>G, XM_005273846.5:c.*2252T>G, XM_005273846.4:c.*2252T>G, XM_005273846.1:c.*2252T>G, XM_011544850.3:c.*2252T>G, XM_011544850.2:c.*2252T>G

Select item 148980609211.

rs1489806092 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 11:60089251 (GRCh38)
11:59856724 (GRCh37)
Canonical SPDI:: NC_000011.10:60089250:A:C
Gene:: MS4A2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.60089251A>C, NC_000011.9:g.59856724A>C, NG_016014.1:g.5588A>C

Select item 148969030112.

rs1489690301 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 11:60087710 (GRCh38)
11:59855183 (GRCh37)
Canonical SPDI:: NC_000011.10:60087709:A:C
Gene:: MS4A2 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.01079/128 (ALFA)
C=0.00021/4 (TOMMO)
C=0.00382/7 (Korea1K)
C=0.00548/16 (KOREAN)
HGVS:: NC_000011.10:g.60087710A>C, NC_000011.9:g.59855183A>C, NG_016014.1:g.4047A>C

Select item 148928387513.

rs1489283875 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 11:60092950 (GRCh38)
11:59860423 (GRCh37)
Canonical SPDI:: NC_000011.10:60092949:T:A
Gene:: MS4A2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000015/4 (TOPMED)
HGVS:: NC_000011.10:g.60092950T>A, NC_000011.9:g.59860423T>A, NG_016014.1:g.9287T>A

Select item 148840195314.

rs1488401953 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:60092408 (GRCh38)
11:59859881 (GRCh37)
Canonical SPDI:: NC_000011.10:60092407:G:C
Gene:: MS4A2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.60092408G>C, NC_000011.9:g.59859881G>C, NG_016014.1:g.8745G>C

Select item 148754947615.

rs1487549476 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:60087105 (GRCh38)
11:59854578 (GRCh37)
Canonical SPDI:: NC_000011.10:60087104:G:A
Gene:: MS4A2 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000011.10:g.60087105G>A, NC_000011.9:g.59854578G>A, NG_016014.1:g.3442G>A, NW_019805498.1:g.180983G>A

Select item 148655452016.

rs1486554520 [Homo sapiens]

Variant type:: DEL
Alleles:: TCATTCTGAGAGTTGCCC>- [Show Flanks]
Chromosome:: 11:60098157 (GRCh38)
11:59865630 (GRCh37)
Canonical SPDI:: NC_000011.10:60098156:TCATTCTGAGAGTTGCCC:
Gene:: MS4A2 (Varview)
Functional Consequence:: 3_prime_UTR_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000011/3 (TOPMED)
-=0.000021/3 (GnomAD)
HGVS:: NC_000011.10:g.60098157_60098174del, NC_000011.9:g.59865630_59865647del, NG_016014.1:g.14494_14511del, NM_000139.5:c.*2501_*2518del, NM_000139.4:c.*2501_*2518del, NM_001256916.2:c.*2501_*2518del, NM_001256916.1:c.*2501_*2518del, XM_005273846.5:c.*2501_*2518del, XM_005273846.4:c.*2501_*2518del, XM_005273846.1:c.*2501_*2518del, XM_011544850.3:c.*2501_*2518del, XM_011544850.2:c.*2501_*2518del

Select item 148651257617.

rs1486512576 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:60087310 (GRCh38)
11:59854783 (GRCh37)
Canonical SPDI:: NC_000011.10:60087309:C:T
Gene:: MS4A2 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000142/2 (ALFA)
T=0.000029/4 (GnomAD)
T=0.000053/14 (TOPMED)
HGVS:: NC_000011.10:g.60087310C>T, NC_000011.9:g.59854783C>T, NG_016014.1:g.3647C>T

Select item 148588202218.

rs1485882022 has merged into rs546397764 [Homo sapiens]

Variant type:: DELINS
Alleles:: AA>-,A,AAA,AAAA [Show Flanks]
Chromosome:: 11:60087205 (GRCh38)
11:59854678 (GRCh37)
Canonical SPDI:: NC_000011.10:60087195:AAAAAAAAAAA:AAAAAAAAA,NC_000011.10:60087195:AAAAAAAAAAA:AAAAAAAAAA,NC_000011.10:60087195:AAAAAAAAAAA:AAAAAAAAAAAA,NC_000011.10:60087195:AAAAAAAAAAA:AAAAAAAAAAAAA
Gene:: MS4A2 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAA=0./0 (ALFA)
A=0.025/1 (GENOME_DK)
A=0.03846/23 (NorthernSweden)
A=0.09505/476 (1000Genomes)
HGVS:: NC_000011.10:g.60087205_60087206del, NC_000011.10:g.60087206del, NC_000011.10:g.60087206dup, NC_000011.10:g.60087205_60087206dup, NC_000011.9:g.59854678_59854679del, NC_000011.9:g.59854679del, NC_000011.9:g.59854679dup, NC_000011.9:g.59854678_59854679dup, NG_016014.1:g.3542_3543del, NG_016014.1:g.3543del, NG_016014.1:g.3543dup, NG_016014.1:g.3542_3543dup, NW_019805498.1:g.181083_181084del, NW_019805498.1:g.181084del, NW_019805498.1:g.181084dup, NW_019805498.1:g.181083_181084dup

Select item 148488397519.

rs1484883975 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:60097670 (GRCh38)
11:59865143 (GRCh37)
Canonical SPDI:: NC_000011.10:60097669:G:A
Gene:: MS4A2 (Varview)
Functional Consequence:: 3_prime_UTR_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000066/1 (ALFA)
A=0.000014/2 (GnomAD)
A=0.000223/1 (Estonian)
HGVS:: NC_000011.10:g.60097670G>A, NC_000011.9:g.59865143G>A, NG_016014.1:g.14007G>A, NM_000139.5:c.*2014G>A, NM_000139.4:c.*2014G>A, NM_001256916.2:c.*2014G>A, NM_001256916.1:c.*2014G>A, XM_005273846.5:c.*2014G>A, XM_005273846.4:c.*2014G>A, XM_005273846.1:c.*2014G>A, XM_011544850.3:c.*2014G>A, XM_011544850.2:c.*2014G>A

Select item 148483396620.

rs1484833966 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:60095220 (GRCh38)
11:59862693 (GRCh37)
Canonical SPDI:: NC_000011.10:60095219:G:A
Gene:: MS4A2 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000021/3 (GnomAD)
A=0.000026/7 (TOPMED)
HGVS:: NC_000011.10:g.60095220G>A, NC_000011.9:g.59862693G>A, NG_016014.1:g.11557G>A

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