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rs151341279

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341279(-;-)
Make rs151341279(-;C)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324061
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341279
ebirs151341279
HLIrs151341279
Exacrs151341279
Varsomers151341279
Maprs151341279
PheGenIrs151341279
hapmaprs151341279
1000 genomesrs151341279
hgdprs151341279
ensemblrs151341279
gopubmedrs151341279
geneviewrs151341279
scholarrs151341279
googlers151341279
pharmgkbrs151341279
gwascentralrs151341279
openSNPrs151341279
23andMers151341279
23andMe allrs151341279
SNP Nexus

SNPshotrs151341279
SNPdbers151341279
MSV3drs151341279
GWAS Ctlgrs151341279
StatusDeleted
Max Magnitude0
ClinVar
Risk rs151341279(;)
Alt rs151341279(;)
Reference rs151341279(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324061delG
CLNSRC
CLNACC