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rs151341164

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341164(-;-)
Make rs151341164(-;C)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324553
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341164
ebirs151341164
HLIrs151341164
Exacrs151341164
Varsomers151341164
Maprs151341164
PheGenIrs151341164
hapmaprs151341164
1000 genomesrs151341164
hgdprs151341164
ensemblrs151341164
gopubmedrs151341164
geneviewrs151341164
scholarrs151341164
googlers151341164
pharmgkbrs151341164
gwascentralrs151341164
openSNPrs151341164
23andMers151341164
23andMe allrs151341164
SNP Nexus

SNPshotrs151341164
SNPdbers151341164
MSV3drs151341164
GWAS Ctlgrs151341164
StatusDeleted
Max Magnitude0
ClinVar
Risk rs151341164(;)
Alt rs151341164(;)
Reference rs151341164(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324553delG
CLNSRC
CLNACC