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rs151341123

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341123(A;A)
Make rs151341123(A;C)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324596
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341123
ebirs151341123
HLIrs151341123
Exacrs151341123
Varsomers151341123
Maprs151341123
PheGenIrs151341123
hapmaprs151341123
1000 genomesrs151341123
hgdprs151341123
ensemblrs151341123
gopubmedrs151341123
geneviewrs151341123
scholarrs151341123
googlers151341123
pharmgkbrs151341123
gwascentralrs151341123
openSNPrs151341123
23andMers151341123
23andMe allrs151341123
SNP Nexus

SNPshotrs151341123
SNPdbers151341123
MSV3drs151341123
GWAS Ctlgrs151341123
StatusDeleted
Max Magnitude0
ClinVar
Risk rs151341123(A;A)
Alt rs151341123(A;A)
Reference rs151341123(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324596G>T
CLNSRC
CLNACC