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rs151341385

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs151341385(-;-)
Make rs151341385(-;T)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31323097
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341385
ebirs151341385
HLIrs151341385
Exacrs151341385
Varsomers151341385
Maprs151341385
PheGenIrs151341385
hapmaprs151341385
1000 genomesrs151341385
hgdprs151341385
ensemblrs151341385
gopubmedrs151341385
geneviewrs151341385
scholarrs151341385
googlers151341385
pharmgkbrs151341385
gwascentralrs151341385
openSNPrs151341385
23andMers151341385
23andMe allrs151341385
SNP Nexus

SNPshotrs151341385
SNPdbers151341385
MSV3drs151341385
GWAS Ctlgrs151341385
StatusDeleted
Max Magnitude0
ClinVar
Risk rs151341385(;)
Alt rs151341385(;)
Reference rs151341385(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323097delA
CLNSRC
CLNACC