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rs151341266

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs151341266(A;G)
Make rs151341266(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356292
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341266
ebirs151341266
HLIrs151341266
Exacrs151341266
Varsomers151341266
Maprs151341266
PheGenIrs151341266
hapmaprs151341266
1000 genomesrs151341266
hgdprs151341266
ensemblrs151341266
gopubmedrs151341266
geneviewrs151341266
scholarrs151341266
googlers151341266
pharmgkbrs151341266
gwascentralrs151341266
openSNPrs151341266
23andMers151341266
23andMe allrs151341266
SNP Nexus

SNPshotrs151341266
SNPdbers151341266
MSV3drs151341266
GWAS Ctlgrs151341266
Max Magnitude0
ClinVar
Risk rs151341266(C,G;C,G)
Alt rs151341266(C,G;C,G)
Reference rs151341266(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324069T>C; NC_000006.11:g.31324069T>G
CLNSRC
CLNACC