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rs151341292

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs151341292(G;G)
Make rs151341292(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356261
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341292
ebirs151341292
HLIrs151341292
Exacrs151341292
Varsomers151341292
Maprs151341292
PheGenIrs151341292
hapmaprs151341292
1000 genomesrs151341292
hgdprs151341292
ensemblrs151341292
gopubmedrs151341292
geneviewrs151341292
scholarrs151341292
googlers151341292
pharmgkbrs151341292
gwascentralrs151341292
openSNPrs151341292
23andMers151341292
23andMe allrs151341292
SNP Nexus

SNPshotrs151341292
SNPdbers151341292
MSV3drs151341292
GWAS Ctlgrs151341292
Max Magnitude0
ClinVar
Risk rs151341292(G;G)
Alt rs151341292(G;G)
Reference rs151341292(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324038A>C
CLNSRC
CLNACC