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rs151341130

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341130(C;C)
Make rs151341130(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356816
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341130
ebirs151341130
HLIrs151341130
Exacrs151341130
Varsomers151341130
Maprs151341130
PheGenIrs151341130
hapmaprs151341130
1000 genomesrs151341130
hgdprs151341130
ensemblrs151341130
gopubmedrs151341130
geneviewrs151341130
scholarrs151341130
googlers151341130
pharmgkbrs151341130
gwascentralrs151341130
openSNPrs151341130
23andMers151341130
23andMe allrs151341130
SNP Nexus

SNPshotrs151341130
SNPdbers151341130
MSV3drs151341130
GWAS Ctlgrs151341130
Max Magnitude0
ClinVar
Risk rs151341130(C;C)
Alt rs151341130(C;C)
Reference rs151341130(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324593C>G
CLNSRC
CLNACC