Have questions? Visit https://www.reddit.com/r/SNPedia

rs151341368

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341368(-;-)
Make rs151341368(-;C)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31323112
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341368
ebirs151341368
HLIrs151341368
Exacrs151341368
Varsomers151341368
Maprs151341368
PheGenIrs151341368
hapmaprs151341368
1000 genomesrs151341368
hgdprs151341368
ensemblrs151341368
gopubmedrs151341368
geneviewrs151341368
scholarrs151341368
googlers151341368
pharmgkbrs151341368
gwascentralrs151341368
openSNPrs151341368
23andMers151341368
23andMe allrs151341368
SNP Nexus

SNPshotrs151341368
SNPdbers151341368
MSV3drs151341368
GWAS Ctlgrs151341368
StatusDeleted
Max Magnitude0
ClinVar
Risk rs151341368(;)
Alt rs151341368(;)
Reference rs151341368(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323112delG
CLNSRC
CLNACC