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rs151341263

From SNPedia

Merged intors151341262
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341263(C;G)
Make rs151341263(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356293
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341263
ebirs151341263
HLIrs151341263
Exacrs151341263
Varsomers151341263
Maprs151341263
PheGenIrs151341263
hapmaprs151341263
1000 genomesrs151341263
hgdprs151341263
ensemblrs151341263
gopubmedrs151341263
geneviewrs151341263
scholarrs151341263
googlers151341263
pharmgkbrs151341263
gwascentralrs151341263
openSNPrs151341263
23andMers151341263
23andMe allrs151341263
SNP Nexus

SNPshotrs151341263
SNPdbers151341263
MSV3drs151341263
GWAS Ctlgrs151341263
StatusMerged into rs151341262
Max Magnitude0
ClinVar
Risk rs151341263(G;G)
Alt rs151341263(G;G)
Reference rs151341263(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324070G>C
CLNSRC
CLNACC