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rs151341127

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341127(C;G)
Make rs151341127(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356817
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341127
ebirs151341127
HLIrs151341127
Exacrs151341127
Varsomers151341127
Maprs151341127
PheGenIrs151341127
hapmaprs151341127
1000 genomesrs151341127
hgdprs151341127
ensemblrs151341127
gopubmedrs151341127
geneviewrs151341127
scholarrs151341127
googlers151341127
pharmgkbrs151341127
gwascentralrs151341127
openSNPrs151341127
23andMers151341127
23andMe allrs151341127
SNP Nexus

SNPshotrs151341127
SNPdbers151341127
MSV3drs151341127
GWAS Ctlgrs151341127
Merged fromRs151341128
Max Magnitude0
ClinVar
Risk rs151341127(G,T;G,T)
Alt rs151341127(G,T;G,T)
Reference rs151341127(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324594G>A; NC_000006.11:g.31324594G>C
CLNSRC
CLNACC