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rs151341278

From SNPedia

Merged intors151341277
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341278(C;T)
Make rs151341278(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356285
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341278
ebirs151341278
HLIrs151341278
Exacrs151341278
Varsomers151341278
Maprs151341278
PheGenIrs151341278
hapmaprs151341278
1000 genomesrs151341278
hgdprs151341278
ensemblrs151341278
gopubmedrs151341278
geneviewrs151341278
scholarrs151341278
googlers151341278
pharmgkbrs151341278
gwascentralrs151341278
openSNPrs151341278
23andMers151341278
23andMe allrs151341278
SNP Nexus

SNPshotrs151341278
SNPdbers151341278
MSV3drs151341278
GWAS Ctlgrs151341278
StatusMerged into rs151341277
Max Magnitude0
ClinVar
Risk rs151341278(T;T)
Alt rs151341278(T;T)
Reference rs151341278(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324062G>A
CLNSRC
CLNACC