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rs151341379

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341379(-;-)
Make rs151341379(-;C)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31323103
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341379
ebirs151341379
HLIrs151341379
Exacrs151341379
Varsomers151341379
Maprs151341379
PheGenIrs151341379
hapmaprs151341379
1000 genomesrs151341379
hgdprs151341379
ensemblrs151341379
gopubmedrs151341379
geneviewrs151341379
scholarrs151341379
googlers151341379
pharmgkbrs151341379
gwascentralrs151341379
openSNPrs151341379
23andMers151341379
23andMe allrs151341379
SNP Nexus

SNPshotrs151341379
SNPdbers151341379
MSV3drs151341379
GWAS Ctlgrs151341379
StatusDeleted
Max Magnitude0
ClinVar
Risk rs151341379(;)
Alt rs151341379(;)
Reference rs151341379(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323103delG
CLNSRC
CLNACC