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

rs9264619

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs9264619(A;A)
Make rs9264619(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355163
GeneHLA-B
is asnp
is mentioned by
dbSNPrs9264619
ebirs9264619
HLIrs9264619
Exacrs9264619
Varsomers9264619
Maprs9264619
PheGenIrs9264619
hapmaprs9264619
1000 genomesrs9264619
hgdprs9264619
ensemblrs9264619
gopubmedrs9264619
geneviewrs9264619
scholarrs9264619
googlers9264619
pharmgkbrs9264619
gwascentralrs9264619
openSNPrs9264619
23andMers9264619
23andMe allrs9264619
SNP Nexus

SNPshotrs9264619
SNPdbers9264619
MSV3drs9264619
GWAS Ctlgrs9264619
Max Magnitude0
ClinVar
Risk rs9264619(A;A)
Alt rs9264619(A;A)
Reference rs9264619(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31322940G>A
CLNSRC
CLNACC