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rs151341367

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341367(-;-)
Make rs151341367(-;G)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31323113
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341367
ebirs151341367
HLIrs151341367
Exacrs151341367
Varsomers151341367
Maprs151341367
PheGenIrs151341367
hapmaprs151341367
1000 genomesrs151341367
hgdprs151341367
ensemblrs151341367
gopubmedrs151341367
geneviewrs151341367
scholarrs151341367
googlers151341367
pharmgkbrs151341367
gwascentralrs151341367
openSNPrs151341367
23andMers151341367
23andMe allrs151341367
SNP Nexus

SNPshotrs151341367
SNPdbers151341367
MSV3drs151341367
GWAS Ctlgrs151341367
StatusDeleted
Max Magnitude0
ClinVar
Risk rs151341367(;)
Alt rs151341367(;)
Reference rs151341367(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323113delC
CLNSRC
CLNACC