Have questions? Visit https://www.reddit.com/r/SNPedia

rs151341112

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs151341112(G;G)
Make rs151341112(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356858
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341112
ebirs151341112
HLIrs151341112
Exacrs151341112
Varsomers151341112
Maprs151341112
PheGenIrs151341112
hapmaprs151341112
1000 genomesrs151341112
hgdprs151341112
ensemblrs151341112
gopubmedrs151341112
geneviewrs151341112
scholarrs151341112
googlers151341112
pharmgkbrs151341112
gwascentralrs151341112
openSNPrs151341112
23andMers151341112
23andMe allrs151341112
SNP Nexus

SNPshotrs151341112
SNPdbers151341112
MSV3drs151341112
GWAS Ctlgrs151341112
Max Magnitude0
ClinVar
Risk rs151341112(G;G)
Alt rs151341112(G;G)
Reference rs151341112(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324635A>C
CLNSRC
CLNACC