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rs151341182

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341182(C;T)
Make rs151341182(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356768
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341182
ebirs151341182
HLIrs151341182
Exacrs151341182
Varsomers151341182
Maprs151341182
PheGenIrs151341182
hapmaprs151341182
1000 genomesrs151341182
hgdprs151341182
ensemblrs151341182
gopubmedrs151341182
geneviewrs151341182
scholarrs151341182
googlers151341182
pharmgkbrs151341182
gwascentralrs151341182
openSNPrs151341182
23andMers151341182
23andMe allrs151341182
SNP Nexus

SNPshotrs151341182
SNPdbers151341182
MSV3drs151341182
GWAS Ctlgrs151341182
Max Magnitude0
ClinVar
Risk rs151341182(T;T)
Alt rs151341182(T;T)
Reference rs151341182(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324545G>A
CLNSRC
CLNACC