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rs151341113

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs151341113(C;C)
Make rs151341113(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356853
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341113
ebirs151341113
HLIrs151341113
Exacrs151341113
Varsomers151341113
Maprs151341113
PheGenIrs151341113
hapmaprs151341113
1000 genomesrs151341113
hgdprs151341113
ensemblrs151341113
gopubmedrs151341113
geneviewrs151341113
scholarrs151341113
googlers151341113
pharmgkbrs151341113
gwascentralrs151341113
openSNPrs151341113
23andMers151341113
23andMe allrs151341113
SNP Nexus

SNPshotrs151341113
SNPdbers151341113
MSV3drs151341113
GWAS Ctlgrs151341113
Max Magnitude0
ClinVar
Risk rs151341113(C;C)
Alt rs151341113(C;C)
Reference rs151341113(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324630A>G
CLNSRC
CLNACC