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rs9632884

From SNPedia

Orientationplus
Stabilizedplus
Make rs9632884(C;C)
Make rs9632884(C;G)
Make rs9632884(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position22072302
GeneCDKN2B-AS1
is asnp
is mentioned by
dbSNPrs9632884
ebirs9632884
HLIrs9632884
Exacrs9632884
Varsomers9632884
Maprs9632884
PheGenIrs9632884
hapmaprs9632884
1000 genomesrs9632884
hgdprs9632884
ensemblrs9632884
gopubmedrs9632884
geneviewrs9632884
scholarrs9632884
googlers9632884
pharmgkbrs9632884
gwascentralrs9632884
openSNPrs9632884
23andMers9632884
23andMe allrs9632884
SNP Nexus

SNPshotrs9632884
SNPdbers9632884
MSV3drs9632884
GWAS Ctlgrs9632884
GMAF0.332
Max Magnitude
? (C;C) (C;G) (G;G) 28
Rs9632884
PubMed [PMID 17478681OA-icon.png]
Affy Probeset SNP_A-2063543
Affy Orientation same
On GW 5.0 1
Alleles A/B C/G
Ancestral C
Population CEU
Allele C
Case Freq.
Control Freq.
Odds Ratio Het 1.30
Odds Ratio Hom 1.54
Odds Ratio All 1.23
Disease Coronary artery disease (CAD)


rs9632884 increases susceptibility to Coronary artery disease 1.30 times for heterozygotes (CG) and 1.54 times for homozygotes (CC) [PMID 17478681OA-icon.png]