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rs151341134

From SNPedia

Merged intors151341132
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341134(C;T)
Make rs151341134(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356813
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341134
ebirs151341134
HLIrs151341134
Exacrs151341134
Varsomers151341134
Maprs151341134
PheGenIrs151341134
hapmaprs151341134
1000 genomesrs151341134
hgdprs151341134
ensemblrs151341134
gopubmedrs151341134
geneviewrs151341134
scholarrs151341134
googlers151341134
pharmgkbrs151341134
gwascentralrs151341134
openSNPrs151341134
23andMers151341134
23andMe allrs151341134
SNP Nexus

SNPshotrs151341134
SNPdbers151341134
MSV3drs151341134
GWAS Ctlgrs151341134
StatusMerged into rs151341132
Max Magnitude0
ClinVar
Risk rs151341134(T;T)
Alt rs151341134(T;T)
Reference rs151341134(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324590G>A
CLNSRC
CLNACC