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

rs9264597

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs9264597(A;G)
Make rs9264597(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269456
GeneHLA-C
is asnp
is mentioned by
dbSNPrs9264597
ebirs9264597
HLIrs9264597
Exacrs9264597
Varsomers9264597
Maprs9264597
PheGenIrs9264597
hapmaprs9264597
1000 genomesrs9264597
hgdprs9264597
ensemblrs9264597
gopubmedrs9264597
geneviewrs9264597
scholarrs9264597
googlers9264597
pharmgkbrs9264597
gwascentralrs9264597
openSNPrs9264597
23andMers9264597
23andMe allrs9264597
SNP Nexus

SNPshotrs9264597
SNPdbers9264597
MSV3drs9264597
GWAS Ctlgrs9264597
GMAF0.3012
Max Magnitude0
ClinVar
Risk rs9264597(G;G)
Alt rs9264597(G;G)
Reference rs9264597(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31237233A>G
CLNSRC
CLNACC