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rs151341366

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs151341366(-;-)
Make rs151341366(-;A)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31323114
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341366
ebirs151341366
HLIrs151341366
Exacrs151341366
Varsomers151341366
Maprs151341366
PheGenIrs151341366
hapmaprs151341366
1000 genomesrs151341366
hgdprs151341366
ensemblrs151341366
gopubmedrs151341366
geneviewrs151341366
scholarrs151341366
googlers151341366
pharmgkbrs151341366
gwascentralrs151341366
openSNPrs151341366
23andMers151341366
23andMe allrs151341366
SNP Nexus

SNPshotrs151341366
SNPdbers151341366
MSV3drs151341366
GWAS Ctlgrs151341366
StatusDeleted
Max Magnitude0
ClinVar
Risk rs151341366(;)
Alt rs151341366(;)
Reference rs151341366(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323114delT
CLNSRC
CLNACC