Annotation Detail
Information
- Associated Genes
- LEP
- Associated Variants
-
LEP c.-39G>A
(
ENST00000308868.5 )
LEP c.-39G>A ( ENST00000308868.5 ) - Associated Disease
- arteriosclerosis
- Source Database
- DisGeNET
- Description
- LEP rs2167270 polymorphism does not seem to be a genetic risk factor for disease susceptibility or clinically evident CV disease and subclinical atherosclerosis in patients with RA.
- Pubmed
- 21385539
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.00298586059288334
- Year of publication
- 2011
Drugs