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rs151341369

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341369(-;-)
Make rs151341369(-;C)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31323111
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341369
ebirs151341369
HLIrs151341369
Exacrs151341369
Varsomers151341369
Maprs151341369
PheGenIrs151341369
hapmaprs151341369
1000 genomesrs151341369
hgdprs151341369
ensemblrs151341369
gopubmedrs151341369
geneviewrs151341369
scholarrs151341369
googlers151341369
pharmgkbrs151341369
gwascentralrs151341369
openSNPrs151341369
23andMers151341369
23andMe allrs151341369
SNP Nexus

SNPshotrs151341369
SNPdbers151341369
MSV3drs151341369
GWAS Ctlgrs151341369
StatusDeleted
Max Magnitude0
ClinVar
Risk rs151341369(;)
Alt rs151341369(;)
Reference rs151341369(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323111delG
CLNSRC
CLNACC