Have questions? Visit https://www.reddit.com/r/SNPedia

rs151341076

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341076(C;T)
Make rs151341076(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31357087
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341076
ebirs151341076
HLIrs151341076
Exacrs151341076
Varsomers151341076
Maprs151341076
PheGenIrs151341076
hapmaprs151341076
1000 genomesrs151341076
hgdprs151341076
ensemblrs151341076
gopubmedrs151341076
geneviewrs151341076
scholarrs151341076
googlers151341076
pharmgkbrs151341076
gwascentralrs151341076
openSNPrs151341076
23andMers151341076
23andMe allrs151341076
SNP Nexus

SNPshotrs151341076
SNPdbers151341076
MSV3drs151341076
GWAS Ctlgrs151341076
Merged fromRs151341077
GMAF0.07392
Max Magnitude0
ClinVar
Risk rs151341076(G,T;G,T)
Alt rs151341076(G,T;G,T)
Reference rs151341076(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324864G>A; NC_000006.11:g.31324864G>C
CLNSRC
CLNACC