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rs151341089

From SNPedia

Merged intors151341088
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341089(C;G)
Make rs151341089(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356953
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341089
ebirs151341089
HLIrs151341089
Exacrs151341089
Varsomers151341089
Maprs151341089
PheGenIrs151341089
hapmaprs151341089
1000 genomesrs151341089
hgdprs151341089
ensemblrs151341089
gopubmedrs151341089
geneviewrs151341089
scholarrs151341089
googlers151341089
pharmgkbrs151341089
gwascentralrs151341089
openSNPrs151341089
23andMers151341089
23andMe allrs151341089
SNP Nexus

SNPshotrs151341089
SNPdbers151341089
MSV3drs151341089
GWAS Ctlgrs151341089
StatusMerged into rs151341088
Max Magnitude0
ClinVar
Risk rs151341089(G;G)
Alt rs151341089(G;G)
Reference rs151341089(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324730G>C
CLNSRC
CLNACC