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rs151341068

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341068(C;T)
Make rs151341068(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31357342
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341068
ebirs151341068
HLIrs151341068
Exacrs151341068
Varsomers151341068
Maprs151341068
PheGenIrs151341068
hapmaprs151341068
1000 genomesrs151341068
hgdprs151341068
ensemblrs151341068
gopubmedrs151341068
geneviewrs151341068
scholarrs151341068
googlers151341068
pharmgkbrs151341068
gwascentralrs151341068
openSNPrs151341068
23andMers151341068
23andMe allrs151341068
SNP Nexus

SNPshotrs151341068
SNPdbers151341068
MSV3drs151341068
GWAS Ctlgrs151341068
Max Magnitude0
ClinVar
Risk rs151341068(T;T)
Alt rs151341068(T;T)
Reference rs151341068(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31325119G>A
CLNSRC
CLNACC