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rs9264594

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs9264594(A;G)
Make rs9264594(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269271
GeneHLA-C
is asnp
is mentioned by
dbSNPrs9264594
ebirs9264594
HLIrs9264594
Exacrs9264594
Varsomers9264594
Maprs9264594
PheGenIrs9264594
hapmaprs9264594
1000 genomesrs9264594
hgdprs9264594
ensemblrs9264594
gopubmedrs9264594
geneviewrs9264594
scholarrs9264594
googlers9264594
pharmgkbrs9264594
gwascentralrs9264594
openSNPrs9264594
23andMers9264594
23andMe allrs9264594
SNP Nexus

SNPshotrs9264594
SNPdbers9264594
MSV3drs9264594
GWAS Ctlgrs9264594
GMAF0.2208
Max Magnitude0
? (A;A) (A;G) (G;G) 28
ClinVar
Risk rs9264594(G;G)
Alt rs9264594(G;G)
Reference rs9264594(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31237048A>G
CLNSRC
CLNACC