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rs151341378

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341378(-;-)
Make rs151341378(-;C)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31323104
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341378
ebirs151341378
HLIrs151341378
Exacrs151341378
Varsomers151341378
Maprs151341378
PheGenIrs151341378
hapmaprs151341378
1000 genomesrs151341378
hgdprs151341378
ensemblrs151341378
gopubmedrs151341378
geneviewrs151341378
scholarrs151341378
googlers151341378
pharmgkbrs151341378
gwascentralrs151341378
openSNPrs151341378
23andMers151341378
23andMe allrs151341378
SNP Nexus

SNPshotrs151341378
SNPdbers151341378
MSV3drs151341378
GWAS Ctlgrs151341378
StatusDeleted
Max Magnitude0
ClinVar
Risk rs151341378(;)
Alt rs151341378(;)
Reference rs151341378(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323104delG
CLNSRC
CLNACC