cataract Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A lens disease characterized by clouding of the lens inside the eye which leads to a decrease in vision. (Human Disease Ontology, DOID_83)
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4 genes associated with the cataract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
FAM19A1 family with sequence similarity 19 (chemokine (C-C motif)-like), member A1 1.16343
PPARD peroxisome proliferator-activated receptor delta 0.969142
CCDC102A coiled-coil domain containing 102A 0.919744
MAGI1 membrane associated guanylate kinase, WW and PDZ domain containing 1 0.734978