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rs151341389

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341389(C;T)
Make rs151341389(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355204
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341389
ebirs151341389
HLIrs151341389
Exacrs151341389
Varsomers151341389
Maprs151341389
PheGenIrs151341389
hapmaprs151341389
1000 genomesrs151341389
hgdprs151341389
ensemblrs151341389
gopubmedrs151341389
geneviewrs151341389
scholarrs151341389
googlers151341389
pharmgkbrs151341389
gwascentralrs151341389
openSNPrs151341389
23andMers151341389
23andMe allrs151341389
SNP Nexus

SNPshotrs151341389
SNPdbers151341389
MSV3drs151341389
GWAS Ctlgrs151341389
Max Magnitude0
ClinVar
Risk rs151341389(T;T)
Alt rs151341389(T;T)
Reference rs151341389(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322981G>A
CLNSRC
CLNACC