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rs151341254

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341254(C;G)
Make rs151341254(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356310
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341254
ebirs151341254
HLIrs151341254
Exacrs151341254
Varsomers151341254
Maprs151341254
PheGenIrs151341254
hapmaprs151341254
1000 genomesrs151341254
hgdprs151341254
ensemblrs151341254
gopubmedrs151341254
geneviewrs151341254
scholarrs151341254
googlers151341254
pharmgkbrs151341254
gwascentralrs151341254
openSNPrs151341254
23andMers151341254
23andMe allrs151341254
SNP Nexus

SNPshotrs151341254
SNPdbers151341254
MSV3drs151341254
GWAS Ctlgrs151341254
Max Magnitude0
ClinVar
Risk rs151341254(G,T;G,T)
Alt rs151341254(G,T;G,T)
Reference rs151341254(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324087G>A; NC_000006.11:g.31324087G>C
CLNSRC
CLNACC