Annotation Detail
Information
- Associated Genes
- FOLH1
- Associated Variants
-
FOLH1 p.Arg536Trp (p.R536W)
(
ENST00000533034.1,
ENST00000256999.7,
ENST00000356696.7,
ENST00000340334.11 )
FOLH1 p.Arg536Trp (p.R536W) ( ENST00000256999.7, ENST00000340334.11, ENST00000356696.7, ENST00000533034.1 ) - Associated Disease
- coronary artery disease
- Source Database
- DisGeNET
- Description
- GCPII C1561T polymorphism was found to be an independent risk factor (OR 2.71, 95% CI 1.47-4.98) for CAD, whereas cSHMT C1420T conferred protection (OR 0.51, 95% CI 0.37-0.70).
- Pubmed
- 22147344
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.00081432561624091
- Year of publication
- 2014
Drugs