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rs151341078

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341078(-;-)
Make rs151341078(-;G)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324760
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341078
ebirs151341078
HLIrs151341078
Exacrs151341078
Varsomers151341078
Maprs151341078
PheGenIrs151341078
hapmaprs151341078
1000 genomesrs151341078
hgdprs151341078
ensemblrs151341078
gopubmedrs151341078
geneviewrs151341078
scholarrs151341078
googlers151341078
pharmgkbrs151341078
gwascentralrs151341078
openSNPrs151341078
23andMers151341078
23andMe allrs151341078
SNP Nexus

SNPshotrs151341078
SNPdbers151341078
MSV3drs151341078
GWAS Ctlgrs151341078
StatusDeleted
Max Magnitude0
ClinVar
Risk rs151341078(;)
Alt rs151341078(;)
Reference rs151341078(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324760delC
CLNSRC
CLNACC