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rs151341422

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341422(C;T)
Make rs151341422(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354348
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341422
ebirs151341422
HLIrs151341422
Exacrs151341422
Varsomers151341422
Maprs151341422
PheGenIrs151341422
hapmaprs151341422
1000 genomesrs151341422
hgdprs151341422
ensemblrs151341422
gopubmedrs151341422
geneviewrs151341422
scholarrs151341422
googlers151341422
pharmgkbrs151341422
gwascentralrs151341422
openSNPrs151341422
23andMers151341422
23andMe allrs151341422
SNP Nexus

SNPshotrs151341422
SNPdbers151341422
MSV3drs151341422
GWAS Ctlgrs151341422
Max Magnitude0
ClinVar
Risk rs151341422(T;T)
Alt rs151341422(T;T)
Reference rs151341422(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322125G>A
CLNSRC
CLNACC