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rs151341122

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341122(-;-)
Make rs151341122(-;C)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324596
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341122
ebirs151341122
HLIrs151341122
Exacrs151341122
Varsomers151341122
Maprs151341122
PheGenIrs151341122
hapmaprs151341122
1000 genomesrs151341122
hgdprs151341122
ensemblrs151341122
gopubmedrs151341122
geneviewrs151341122
scholarrs151341122
googlers151341122
pharmgkbrs151341122
gwascentralrs151341122
openSNPrs151341122
23andMers151341122
23andMe allrs151341122
SNP Nexus

SNPshotrs151341122
SNPdbers151341122
MSV3drs151341122
GWAS Ctlgrs151341122
StatusDeleted
Max Magnitude0
ClinVar
Risk rs151341122(;)
Alt rs151341122(;)
Reference rs151341122(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324596delG
CLNSRC
CLNACC