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rs151341167

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341167(-;-)
Make rs151341167(-;C)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324552
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341167
ebirs151341167
HLIrs151341167
Exacrs151341167
Varsomers151341167
Maprs151341167
PheGenIrs151341167
hapmaprs151341167
1000 genomesrs151341167
hgdprs151341167
ensemblrs151341167
gopubmedrs151341167
geneviewrs151341167
scholarrs151341167
googlers151341167
pharmgkbrs151341167
gwascentralrs151341167
openSNPrs151341167
23andMers151341167
23andMe allrs151341167
SNP Nexus

SNPshotrs151341167
SNPdbers151341167
MSV3drs151341167
GWAS Ctlgrs151341167
StatusDeleted
Max Magnitude0
ClinVar
Risk rs151341167(;)
Alt rs151341167(;)
Reference rs151341167(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324552delG
CLNSRC
CLNACC