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rs151341093

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341093(C;T)
Make rs151341093(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356935
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341093
ebirs151341093
HLIrs151341093
Exacrs151341093
Varsomers151341093
Maprs151341093
PheGenIrs151341093
hapmaprs151341093
1000 genomesrs151341093
hgdprs151341093
ensemblrs151341093
gopubmedrs151341093
geneviewrs151341093
scholarrs151341093
googlers151341093
pharmgkbrs151341093
gwascentralrs151341093
openSNPrs151341093
23andMers151341093
23andMe allrs151341093
SNP Nexus

SNPshotrs151341093
SNPdbers151341093
MSV3drs151341093
GWAS Ctlgrs151341093
Max Magnitude0
ClinVar
Risk rs151341093(T;T)
Alt rs151341093(T;T)
Reference rs151341093(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324712G>A
CLNSRC
CLNACC