SNP Links for Nucleotide (Select 1137644261) - SNP

Links from Nucleotide

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Select item 14912707841.

rs1491270784 has merged into rs56101324 [Homo sapiens]

Variant type:: DELINS
Alleles:: GG>-,G,GGG,GGGG,GGGGG,GGGGGG,GGGGGGG,GGGGGGGG,GGGGGGGGG,GGGGGGGGGG,GGGGGGGGGGG,GGGGGGGGGGGG,GGGGGGGGGGGGG,GGGGGGGGGGGGGG,GGGGGGGGGGGGGGG,GGGGGGGGGGGGGGGG,GGGGGGGGGGGGGGGGG,GGGGGGGGGGGGGGGGGG,GGGGGGGGGGGGGGGGGGG [Show Flanks]
Chromosome:: 6:35738295 (GRCh38)
6:35706072 (GRCh37)
Canonical SPDI:: NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGG,NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGG,NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGG,NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGG,NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGG,NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGGG,NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGGGG,NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGGGGG,NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGGGGGG,NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGGGGGGG,NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGGGGGGGG,NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGGGGGGGGG,NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGG,NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGG,NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGG,NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGG,NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGGG,NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGGGG,NC_000006.12:35738286:GGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGGGGG
Gene:: ARMC12 (Varview), LOC285847 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GGGGGGGGG=0./0 (ALFA)
-=0.2049/1026 (1000Genomes)
HGVS:: NC_000006.12:g.35738295_35738296del, NC_000006.12:g.35738296del, NC_000006.12:g.35738296dup, NC_000006.12:g.35738295_35738296dup, NC_000006.12:g.35738294_35738296dup, NC_000006.12:g.35738293_35738296dup, NC_000006.12:g.35738292_35738296dup, NC_000006.12:g.35738291_35738296dup, NC_000006.12:g.35738290_35738296dup, NC_000006.12:g.35738289_35738296dup, NC_000006.12:g.35738288_35738296dup, NC_000006.12:g.35738287_35738296dup, NC_000006.12:g.35738296_35738297insGGGGGGGGGGG, NC_000006.12:g.35738296_35738297insGGGGGGGGGGGG, NC_000006.12:g.35738296_35738297insGGGGGGGGGGGGG, NC_000006.12:g.35738296_35738297insGGGGGGGGGGGGGG, NC_000006.12:g.35738296_35738297insGGGGGGGGGGGGGGG, NC_000006.12:g.35738296_35738297insGGGGGGGGGGGGGGGG, NC_000006.12:g.35738296_35738297insGGGGGGGGGGGGGGGGG, NC_000006.11:g.35706072_35706073del, NC_000006.11:g.35706073del, NC_000006.11:g.35706073dup, NC_000006.11:g.35706072_35706073dup, NC_000006.11:g.35706071_35706073dup, NC_000006.11:g.35706070_35706073dup, NC_000006.11:g.35706069_35706073dup, NC_000006.11:g.35706068_35706073dup, NC_000006.11:g.35706067_35706073dup, NC_000006.11:g.35706066_35706073dup, NC_000006.11:g.35706065_35706073dup, NC_000006.11:g.35706064_35706073dup, NC_000006.11:g.35706073_35706074insGGGGGGGGGGG, NC_000006.11:g.35706073_35706074insGGGGGGGGGGGG, NC_000006.11:g.35706073_35706074insGGGGGGGGGGGGG, NC_000006.11:g.35706073_35706074insGGGGGGGGGGGGGG, NC_000006.11:g.35706073_35706074insGGGGGGGGGGGGGGG, NC_000006.11:g.35706073_35706074insGGGGGGGGGGGGGGGG, NC_000006.11:g.35706073_35706074insGGGGGGGGGGGGGGGGG, NG_052798.1:g.9570_9571del, NG_052798.1:g.9571del, NG_052798.1:g.9571dup, NG_052798.1:g.9570_9571dup, NG_052798.1:g.9569_9571dup, NG_052798.1:g.9568_9571dup, NG_052798.1:g.9567_9571dup, NG_052798.1:g.9566_9571dup, NG_052798.1:g.9565_9571dup, NG_052798.1:g.9564_9571dup, NG_052798.1:g.9563_9571dup, NG_052798.1:g.9562_9571dup, NG_052798.1:g.9571_9572insGGGGGGGGGGG, NG_052798.1:g.9571_9572insGGGGGGGGGGGG, NG_052798.1:g.9571_9572insGGGGGGGGGGGGG, NG_052798.1:g.9571_9572insGGGGGGGGGGGGGG, NG_052798.1:g.9571_9572insGGGGGGGGGGGGGGG, NG_052798.1:g.9571_9572insGGGGGGGGGGGGGGGG, NG_052798.1:g.9571_9572insGGGGGGGGGGGGGGGGG

Select item 14911497962.

rs1491149796 has merged into rs11365534 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 6:35740912 (GRCh38)
6:35708689 (GRCh37)
Canonical SPDI:: NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:35740897:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: ARMC12 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000006.12:g.35740912_35740917del, NC_000006.12:g.35740913_35740917del, NC_000006.12:g.35740914_35740917del, NC_000006.12:g.35740915_35740917del, NC_000006.12:g.35740916_35740917del, NC_000006.12:g.35740917del, NC_000006.12:g.35740917dup, NC_000006.12:g.35740916_35740917dup, NC_000006.12:g.35740915_35740917dup, NC_000006.12:g.35740914_35740917dup, NC_000006.12:g.35740913_35740917dup, NC_000006.12:g.35740912_35740917dup, NC_000006.12:g.35740911_35740917dup, NC_000006.12:g.35740910_35740917dup, NC_000006.12:g.35740909_35740917dup, NC_000006.12:g.35740908_35740917dup, NC_000006.12:g.35740904_35740917dup, NC_000006.11:g.35708689_35708694del, NC_000006.11:g.35708690_35708694del, NC_000006.11:g.35708691_35708694del, NC_000006.11:g.35708692_35708694del, NC_000006.11:g.35708693_35708694del, NC_000006.11:g.35708694del, NC_000006.11:g.35708694dup, NC_000006.11:g.35708693_35708694dup, NC_000006.11:g.35708692_35708694dup, NC_000006.11:g.35708691_35708694dup, NC_000006.11:g.35708690_35708694dup, NC_000006.11:g.35708689_35708694dup, NC_000006.11:g.35708688_35708694dup, NC_000006.11:g.35708687_35708694dup, NC_000006.11:g.35708686_35708694dup, NC_000006.11:g.35708685_35708694dup, NC_000006.11:g.35708681_35708694dup, NG_052798.1:g.12187_12192del, NG_052798.1:g.12188_12192del, NG_052798.1:g.12189_12192del, NG_052798.1:g.12190_12192del, NG_052798.1:g.12191_12192del, NG_052798.1:g.12192del, NG_052798.1:g.12192dup, NG_052798.1:g.12191_12192dup, NG_052798.1:g.12190_12192dup, NG_052798.1:g.12189_12192dup, NG_052798.1:g.12188_12192dup, NG_052798.1:g.12187_12192dup, NG_052798.1:g.12186_12192dup, NG_052798.1:g.12185_12192dup, NG_052798.1:g.12184_12192dup, NG_052798.1:g.12183_12192dup, NG_052798.1:g.12179_12192dup

Select item 14908089883.

rs1490808988 [Homo sapiens]

Variant type:: DELINS
Alleles:: AGAT>- [Show Flanks]
Chromosome:: 6:35745514 (GRCh38)
6:35713291 (GRCh37)
Canonical SPDI:: NC_000006.12:35745509:AGATAGAT:AGAT
Gene:: ARMC12 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AGATAGAT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.35745510AGAT[1], NC_000006.11:g.35713287AGAT[1], NG_052798.1:g.16785AGAT[1]

Select item 14907504014.

rs1490750401 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:35730125 (GRCh38)
6:35697902 (GRCh37)
Canonical SPDI:: NC_000006.12:35730124:C:T
Gene:: FKBP5 (Varview), ARMC12 (Varview), LOC285847 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000006.12:g.35730125C>T, NC_000006.11:g.35697902C>T, NG_012645.2:g.3459G>A, NG_052798.1:g.1400C>T

Select item 14906086255.

rs1490608625 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 6:35743930 (GRCh38)
6:35711707 (GRCh37)
Canonical SPDI:: NC_000006.12:35743929:A:C,NC_000006.12:35743929:A:G
Gene:: ARMC12 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.35743930A>C, NC_000006.12:g.35743930A>G, NC_000006.11:g.35711707A>C, NC_000006.11:g.35711707A>G, NG_052798.1:g.15205A>C, NG_052798.1:g.15205A>G

Select item 14905626746.

rs1490562674 [Homo sapiens]

Variant type:: DELINS
Alleles:: GTG>- [Show Flanks]
Chromosome:: 6:35728773 (GRCh38)
6:35696550 (GRCh37)
Canonical SPDI:: NC_000006.12:35728769:GTGGTG:GTG
Gene:: FKBP5 (Varview), LOC285847 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: GTGGTG=0./0 (ALFA)
-=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.35728770GTG[1], NC_000006.11:g.35696547GTG[1], NG_012645.2:g.4809CAC[1], NG_052798.1:g.45GTG[1]

Select item 14903364417.

rs1490336441 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 6:35736390 (GRCh38)
6:35704167 (GRCh37)
Canonical SPDI:: NC_000006.12:35736389:G:T
Gene:: ARMC12 (Varview), LOC285847 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,5_prime_UTR_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000071/1 (TOMMO)
T=0.000546/1 (Korea1K)
HGVS:: NC_000006.12:g.35736390G>T, NC_000006.11:g.35704167G>T, NG_052798.1:g.7665G>T, XM_047418347.1:c.-719G>T

Select item 14901602728.

rs1490160272 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:35744683 (GRCh38)
6:35712460 (GRCh37)
Canonical SPDI:: NC_000006.12:35744682:A:G
Gene:: ARMC12 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000026/7 (TOPMED)
HGVS:: NC_000006.12:g.35744683A>G, NC_000006.11:g.35712460A>G, NG_052798.1:g.15958A>G

Select item 14901110139.

rs1490111013 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 6:35746982 (GRCh38)
6:35714759 (GRCh37)
Canonical SPDI:: NC_000006.12:35746981:T:G
Gene:: ARMC12 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000015/2 (GnomAD)
HGVS:: NC_000006.12:g.35746982T>G, NC_000006.11:g.35714759T>G, NG_052798.1:g.18257T>G

Select item 148994715310.

rs1489947153 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:35748227 (GRCh38)
6:35716004 (GRCh37)
Canonical SPDI:: NC_000006.12:35748226:C:T
Gene:: ARMC12 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
HGVS:: NC_000006.12:g.35748227C>T, NC_000006.11:g.35716004C>T, NG_052798.1:g.19502C>T

Select item 148989570311.

rs1489895703 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 6:35736794 (GRCh38)
6:35704571 (GRCh37)
Canonical SPDI:: NC_000006.12:35736793:G:C
Gene:: ARMC12 (Varview), LOC285847 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,5_prime_UTR_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0./0 (GnomAD)
C=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.35736794G>C, NC_000006.11:g.35704571G>C, NG_052798.1:g.8069G>C, XM_047418347.1:c.-315G>C

Select item 148968242412.

rs1489682424 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:35730075 (GRCh38)
6:35697852 (GRCh37)
Canonical SPDI:: NC_000006.12:35730074:A:G
Gene:: FKBP5 (Varview), ARMC12 (Varview), LOC285847 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency
MAF:: G=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.35730075A>G, NC_000006.11:g.35697852A>G, NG_012645.2:g.3509T>C, NG_052798.1:g.1350A>G

Select item 148906653713.

rs1489066537 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 6:35739637 (GRCh38)
6:35707414 (GRCh37)
Canonical SPDI:: NC_000006.12:35739636:G:A,NC_000006.12:35739636:G:C
Gene:: ARMC12 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0./0 (GnomAD)
C=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.35739637G>A, NC_000006.12:g.35739637G>C, NC_000006.11:g.35707414G>A, NC_000006.11:g.35707414G>C, NG_052798.1:g.10912G>A, NG_052798.1:g.10912G>C

Select item 148898482314.

rs1488984823 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 6:35738529 (GRCh38)
6:35706306 (GRCh37)
Canonical SPDI:: NC_000006.12:35738528:G:C
Gene:: ARMC12 (Varview), LOC285847 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000015/4 (TOPMED)
HGVS:: NC_000006.12:g.35738529G>C, NC_000006.11:g.35706306G>C, NG_052798.1:g.9804G>C

Select item 148883465415.

rs1488834654 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 6:35731609 (GRCh38)
6:35699386 (GRCh37)
Canonical SPDI:: NC_000006.12:35731608:G:A,NC_000006.12:35731608:G:C,NC_000006.12:35731608:G:T
Gene:: ARMC12 (Varview), LOC285847 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,5_prime_UTR_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
C=0.000223/1 (Estonian)
HGVS:: NC_000006.12:g.35731609G>A, NC_000006.12:g.35731609G>C, NC_000006.12:g.35731609G>T, NC_000006.11:g.35699386G>A, NC_000006.11:g.35699386G>C, NC_000006.11:g.35699386G>T, NG_012645.2:g.1975C>T, NG_012645.2:g.1975C>G, NG_012645.2:g.1975C>A, NG_052798.1:g.2884G>A, NG_052798.1:g.2884G>C, NG_052798.1:g.2884G>T, XM_017010435.3:c.-2268G>A, XM_017010435.3:c.-2268G>C, XM_017010435.3:c.-2268G>T, XM_047418347.1:c.-3057G>A, XM_047418347.1:c.-3057G>C, XM_047418347.1:c.-3057G>T, XM_047418343.1:c.-1312G>A, XM_047418343.1:c.-1312G>C, XM_047418343.1:c.-1312G>T, XM_047418344.1:c.-199G>A, XM_047418344.1:c.-199G>C, XM_047418344.1:c.-199G>T

Select item 148873971916.

rs1488739719 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:35750470 (GRCh38)
6:35718247 (GRCh37)
Canonical SPDI:: NC_000006.12:35750469:G:A
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000006.12:g.35750470G>A, NC_000006.11:g.35718247G>A, NG_052798.1:g.21745G>A

Select item 148853590317.

rs1488535903 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:35747065 (GRCh38)
6:35714842 (GRCh37)
Canonical SPDI:: NC_000006.12:35747064:A:G
Gene:: ARMC12 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000011/3 (TOPMED)
HGVS:: NC_000006.12:g.35747065A>G, NC_000006.11:g.35714842A>G, NG_052798.1:g.18340A>G

Select item 148851902118.

rs1488519021 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:35745978 (GRCh38)
6:35713755 (GRCh37)
Canonical SPDI:: NC_000006.12:35745977:A:G
Gene:: ARMC12 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.35745978A>G, NC_000006.11:g.35713755A>G, NG_052798.1:g.17253A>G

Select item 148825953019.

rs1488259530 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:35745908 (GRCh38)
6:35713685 (GRCh37)
Canonical SPDI:: NC_000006.12:35745907:C:T
Gene:: ARMC12 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000011/3 (TOPMED)
HGVS:: NC_000006.12:g.35745908C>T, NC_000006.11:g.35713685C>T, NG_052798.1:g.17183C>T

Select item 148811238420.

rs1488112384 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:35730599 (GRCh38)
6:35698376 (GRCh37)
Canonical SPDI:: NC_000006.12:35730598:G:A
Gene:: ARMC12 (Varview), LOC285847 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000006.12:g.35730599G>A, NC_000006.11:g.35698376G>A, NG_012645.2:g.2985C>T, NG_052798.1:g.1874G>A

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