heterochromia iridis Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Heterochromia iridis is a difference in the color of the iris in the two eyes. (Human Phenotype Ontology, HP_0001100)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0001100
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Genes

3 genes associated with the heterochromia iridis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
GABRG3 gamma-aminobutyric acid (GABA) A receptor, gamma 3 4.07717
OCA2 oculocutaneous albinism II 3.8808
HERC2 HECT and RLD domain containing E3 ubiquitin protein ligase 2 2.49338