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rs151341347

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341347(C;T)
Make rs151341347(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355525
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341347
ebirs151341347
HLIrs151341347
Exacrs151341347
Varsomers151341347
Maprs151341347
PheGenIrs151341347
hapmaprs151341347
1000 genomesrs151341347
hgdprs151341347
ensemblrs151341347
gopubmedrs151341347
geneviewrs151341347
scholarrs151341347
googlers151341347
pharmgkbrs151341347
gwascentralrs151341347
openSNPrs151341347
23andMers151341347
23andMe allrs151341347
SNP Nexus

SNPshotrs151341347
SNPdbers151341347
MSV3drs151341347
GWAS Ctlgrs151341347
Max Magnitude0
ClinVar
Risk rs151341347(T;T)
Alt rs151341347(T;T)
Reference rs151341347(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323302G>A
CLNSRC
CLNACC