Coronary artery disease Gene Set

Dataset GWAS Catalog SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles. (Human Disease Ontology, DOID_3393)
External Link artery disease
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13 genes associated with the Coronary artery disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
PHACTR1 phosphatase and actin regulator 1 0.626595
SMARCA4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 0.626595
ZC3HC1 zinc finger, C3HC-type containing 1 0.560615
TCF21 transcription factor 21 0.499091
PPAP2B phosphatidic acid phosphatase type 2B 0.434785
WDR12 WD repeat domain 12 0.405958
SMG6 SMG6 nonsense mediated mRNA decay factor 0.342586
MRAS muscle RAS oncogene homolog 0.342586
LPL lipoprotein lipase 0.295129
SH2B3 SH2B adaptor protein 3 0.22914
SLC22A3 solute carrier family 22 (organic cation transporter), member 3 0.220915
CNNM2 cyclin and CBS domain divalent metal cation transport mediator 2 0.220915
ANKS1A ankyrin repeat and sterile alpha motif domain containing 1A 0.070053