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rs151341119

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341119(C;G)
Make rs151341119(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356837
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341119
ebirs151341119
HLIrs151341119
Exacrs151341119
Varsomers151341119
Maprs151341119
PheGenIrs151341119
hapmaprs151341119
1000 genomesrs151341119
hgdprs151341119
ensemblrs151341119
gopubmedrs151341119
geneviewrs151341119
scholarrs151341119
googlers151341119
pharmgkbrs151341119
gwascentralrs151341119
openSNPrs151341119
23andMers151341119
23andMe allrs151341119
SNP Nexus

SNPshotrs151341119
SNPdbers151341119
MSV3drs151341119
GWAS Ctlgrs151341119
Max Magnitude0
ClinVar
Risk rs151341119(G,T;G,T)
Alt rs151341119(G,T;G,T)
Reference rs151341119(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324614G>A; NC_000006.11:g.31324614G>C
CLNSRC
CLNACC