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rs151341087

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341087(C;T)
Make rs151341087(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356954
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341087
ebirs151341087
HLIrs151341087
Exacrs151341087
Varsomers151341087
Maprs151341087
PheGenIrs151341087
hapmaprs151341087
1000 genomesrs151341087
hgdprs151341087
ensemblrs151341087
gopubmedrs151341087
geneviewrs151341087
scholarrs151341087
googlers151341087
pharmgkbrs151341087
gwascentralrs151341087
openSNPrs151341087
23andMers151341087
23andMe allrs151341087
SNP Nexus

SNPshotrs151341087
SNPdbers151341087
MSV3drs151341087
GWAS Ctlgrs151341087
Max Magnitude0
ClinVar
Risk rs151341087(T;T)
Alt rs151341087(T;T)
Reference rs151341087(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324731G>A
CLNSRC
CLNACC