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rs9264608

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs9264608(A;G)
Make rs9264608(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269883
GeneHLA-C
is asnp
is mentioned by
dbSNPrs9264608
ebirs9264608
HLIrs9264608
Exacrs9264608
Varsomers9264608
Maprs9264608
PheGenIrs9264608
hapmaprs9264608
1000 genomesrs9264608
hgdprs9264608
ensemblrs9264608
gopubmedrs9264608
geneviewrs9264608
scholarrs9264608
googlers9264608
pharmgkbrs9264608
gwascentralrs9264608
openSNPrs9264608
23andMers9264608
23andMe allrs9264608
SNP Nexus

SNPshotrs9264608
SNPdbers9264608
MSV3drs9264608
GWAS Ctlgrs9264608
GMAF0.2218
Max Magnitude0
? (A;A) (A;G) (G;G) 28
ClinVar
Risk rs9264608(C,G,T;C,G,T)
Alt rs9264608(C,G,T;C,G,T)
Reference rs9264608(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31237660A>G
CLNSRC
CLNACC