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rs151341162

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs151341162(C;C)
Make rs151341162(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356782
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341162
ebirs151341162
HLIrs151341162
Exacrs151341162
Varsomers151341162
Maprs151341162
PheGenIrs151341162
hapmaprs151341162
1000 genomesrs151341162
hgdprs151341162
ensemblrs151341162
gopubmedrs151341162
geneviewrs151341162
scholarrs151341162
googlers151341162
pharmgkbrs151341162
gwascentralrs151341162
openSNPrs151341162
23andMers151341162
23andMe allrs151341162
SNP Nexus

SNPshotrs151341162
SNPdbers151341162
MSV3drs151341162
GWAS Ctlgrs151341162
Max Magnitude0
ClinVar
Risk rs151341162(C;C)
Alt rs151341162(C;C)
Reference rs151341162(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324559A>G
CLNSRC
CLNACC