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rs151341281

From SNPedia

Merged intors151341280
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341281(C;T)
Make rs151341281(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356284
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341281
ebirs151341281
HLIrs151341281
Exacrs151341281
Varsomers151341281
Maprs151341281
PheGenIrs151341281
hapmaprs151341281
1000 genomesrs151341281
hgdprs151341281
ensemblrs151341281
gopubmedrs151341281
geneviewrs151341281
scholarrs151341281
googlers151341281
pharmgkbrs151341281
gwascentralrs151341281
openSNPrs151341281
23andMers151341281
23andMe allrs151341281
SNP Nexus

SNPshotrs151341281
SNPdbers151341281
MSV3drs151341281
GWAS Ctlgrs151341281
StatusMerged into rs151341280
Max Magnitude0
ClinVar
Risk rs151341281(T;T)
Alt rs151341281(T;T)
Reference rs151341281(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324061G>A
CLNSRC
CLNACC