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rs151341114

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341114(C;G)
Make rs151341114(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356851
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341114
ebirs151341114
HLIrs151341114
Exacrs151341114
Varsomers151341114
Maprs151341114
PheGenIrs151341114
hapmaprs151341114
1000 genomesrs151341114
hgdprs151341114
ensemblrs151341114
gopubmedrs151341114
geneviewrs151341114
scholarrs151341114
googlers151341114
pharmgkbrs151341114
gwascentralrs151341114
openSNPrs151341114
23andMers151341114
23andMe allrs151341114
SNP Nexus

SNPshotrs151341114
SNPdbers151341114
MSV3drs151341114
GWAS Ctlgrs151341114
Max Magnitude0
ClinVar
Risk rs151341114(G,T;G,T)
Alt rs151341114(G,T;G,T)
Reference rs151341114(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324628G>A; NC_000006.11:g.31324628G>C
CLNSRC
CLNACC