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rs151341387

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341387(-;-)
Make rs151341387(-;G)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31323095
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341387
ebirs151341387
HLIrs151341387
Exacrs151341387
Varsomers151341387
Maprs151341387
PheGenIrs151341387
hapmaprs151341387
1000 genomesrs151341387
hgdprs151341387
ensemblrs151341387
gopubmedrs151341387
geneviewrs151341387
scholarrs151341387
googlers151341387
pharmgkbrs151341387
gwascentralrs151341387
openSNPrs151341387
23andMers151341387
23andMe allrs151341387
SNP Nexus

SNPshotrs151341387
SNPdbers151341387
MSV3drs151341387
GWAS Ctlgrs151341387
StatusDeleted
Max Magnitude0
ClinVar
Risk rs151341387(;)
Alt rs151341387(;)
Reference rs151341387(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323095delC
CLNSRC
CLNACC