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

rs151341317

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341317(C;C)
Make rs151341317(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356225
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341317
ebirs151341317
HLIrs151341317
Exacrs151341317
Varsomers151341317
Maprs151341317
PheGenIrs151341317
hapmaprs151341317
1000 genomesrs151341317
hgdprs151341317
ensemblrs151341317
gopubmedrs151341317
geneviewrs151341317
scholarrs151341317
googlers151341317
pharmgkbrs151341317
gwascentralrs151341317
openSNPrs151341317
23andMers151341317
23andMe allrs151341317
SNP Nexus

SNPshotrs151341317
SNPdbers151341317
MSV3drs151341317
GWAS Ctlgrs151341317
Max Magnitude0
ClinVar
Risk rs151341317(C;C)
Alt rs151341317(C;C)
Reference rs151341317(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324002C>G
CLNSRC
CLNACC