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rs151341372

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341372(C;T)
Make rs151341372(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355333
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341372
ebirs151341372
HLIrs151341372
Exacrs151341372
Varsomers151341372
Maprs151341372
PheGenIrs151341372
hapmaprs151341372
1000 genomesrs151341372
hgdprs151341372
ensemblrs151341372
gopubmedrs151341372
geneviewrs151341372
scholarrs151341372
googlers151341372
pharmgkbrs151341372
gwascentralrs151341372
openSNPrs151341372
23andMers151341372
23andMe allrs151341372
SNP Nexus

SNPshotrs151341372
SNPdbers151341372
MSV3drs151341372
GWAS Ctlgrs151341372
Max Magnitude0
ClinVar
Risk rs151341372(T;T)
Alt rs151341372(T;T)
Reference rs151341372(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323110G>A
CLNSRC
CLNACC