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rs9264596

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs9264596(A;G)
Make rs9264596(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269453
GeneHLA-C
is asnp
is mentioned by
dbSNPrs9264596
ebirs9264596
HLIrs9264596
Exacrs9264596
Varsomers9264596
Maprs9264596
PheGenIrs9264596
hapmaprs9264596
1000 genomesrs9264596
hgdprs9264596
ensemblrs9264596
gopubmedrs9264596
geneviewrs9264596
scholarrs9264596
googlers9264596
pharmgkbrs9264596
gwascentralrs9264596
openSNPrs9264596
23andMers9264596
23andMe allrs9264596
SNP Nexus

SNPshotrs9264596
SNPdbers9264596
MSV3drs9264596
GWAS Ctlgrs9264596
GMAF0.2815
Max Magnitude0
ClinVar
Risk rs9264596(G;G)
Alt rs9264596(G;G)
Reference rs9264596(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31237230A>G
CLNSRC
CLNACC