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rs151341133

From SNPedia

Merged intors151341132
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341133(C;G)
Make rs151341133(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356813
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341133
ebirs151341133
HLIrs151341133
Exacrs151341133
Varsomers151341133
Maprs151341133
PheGenIrs151341133
hapmaprs151341133
1000 genomesrs151341133
hgdprs151341133
ensemblrs151341133
gopubmedrs151341133
geneviewrs151341133
scholarrs151341133
googlers151341133
pharmgkbrs151341133
gwascentralrs151341133
openSNPrs151341133
23andMers151341133
23andMe allrs151341133
SNP Nexus

SNPshotrs151341133
SNPdbers151341133
MSV3drs151341133
GWAS Ctlgrs151341133
StatusMerged into rs151341132
Max Magnitude0
ClinVar
Risk rs151341133(G;G)
Alt rs151341133(G;G)
Reference rs151341133(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324590G>C
CLNSRC
CLNACC