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rs151341386

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341386(-;-)
Make rs151341386(-;G)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31323096
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341386
ebirs151341386
HLIrs151341386
Exacrs151341386
Varsomers151341386
Maprs151341386
PheGenIrs151341386
hapmaprs151341386
1000 genomesrs151341386
hgdprs151341386
ensemblrs151341386
gopubmedrs151341386
geneviewrs151341386
scholarrs151341386
googlers151341386
pharmgkbrs151341386
gwascentralrs151341386
openSNPrs151341386
23andMers151341386
23andMe allrs151341386
SNP Nexus

SNPshotrs151341386
SNPdbers151341386
MSV3drs151341386
GWAS Ctlgrs151341386
StatusDeleted
Max Magnitude0
ClinVar
Risk rs151341386(;)
Alt rs151341386(;)
Reference rs151341386(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323096delC
CLNSRC
CLNACC