| Dataset | GAD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | A hydroxycoumarin that is 4-hydroxycoumarin which is substituted at position 3 by a 1-phenyl-3-oxo-1-butyl group. (Chemical Entities of Biological Interest Ontology, CHEBI_10033) |
| Similar Terms | |
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6 genes associated with the disease warfarin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| CACNA1C | calcium channel, voltage-dependent, L type, alpha 1C subunit |
| CDHR3 | cadherin-related family member 3 |
| CYP2C9 | cytochrome P450, family 2, subfamily C, polypeptide 9 |
| CYP4F2 | cytochrome P450, family 4, subfamily F, polypeptide 2 |
| STX4 | syntaxin 4 |
| VKORC1 | vitamin K epoxide reductase complex, subunit 1 |
