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rs151341357

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs151341357(C;C)
Make rs151341357(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355390
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341357
ebirs151341357
HLIrs151341357
Exacrs151341357
Varsomers151341357
Maprs151341357
PheGenIrs151341357
hapmaprs151341357
1000 genomesrs151341357
hgdprs151341357
ensemblrs151341357
gopubmedrs151341357
geneviewrs151341357
scholarrs151341357
googlers151341357
pharmgkbrs151341357
gwascentralrs151341357
openSNPrs151341357
23andMers151341357
23andMe allrs151341357
SNP Nexus

SNPshotrs151341357
SNPdbers151341357
MSV3drs151341357
GWAS Ctlgrs151341357
Max Magnitude0
ClinVar
Risk rs151341357(C;C)
Alt rs151341357(C;C)
Reference rs151341357(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323167A>G
CLNSRC
CLNACC