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rs151341077

From SNPedia

Merged intors151341076
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341077(C;T)
Make rs151341077(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31357087
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341077
ebirs151341077
HLIrs151341077
Exacrs151341077
Varsomers151341077
Maprs151341077
PheGenIrs151341077
hapmaprs151341077
1000 genomesrs151341077
hgdprs151341077
ensemblrs151341077
gopubmedrs151341077
geneviewrs151341077
scholarrs151341077
googlers151341077
pharmgkbrs151341077
gwascentralrs151341077
openSNPrs151341077
23andMers151341077
23andMe allrs151341077
SNP Nexus

SNPshotrs151341077
SNPdbers151341077
MSV3drs151341077
GWAS Ctlgrs151341077
StatusMerged into rs151341076
Max Magnitude0
ClinVar
Risk rs151341077(T;T)
Alt rs151341077(T;T)
Reference rs151341077(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324864G>A
CLNSRC
CLNACC