Annotation Detail
Information
- Associated Genes
- MTHFD1L
- Associated Variants
-
MTHFD1L c.1260-4955G>A
(
ENST00000367321.8,
ENST00000611279.4,
ENST00000618312.4 )
MTHFD1L c.1260-4955G>A ( ENST00000367321.8, ENST00000611279.4, ENST00000618312.4 ) - Associated Disease
- Acute coronary syndrome
- Source Database
- DisGeNET
- Description
- After Cox adjustment for other ACS risk factors, of 95 SNPs tested in 811 whites only the association with the rs6922269 in MTHFD1L was statistically significant, with a 2.6-fold mortality hazard (P = 0.007).
- Pubmed
- 21957892
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.000542883744160607
- Year of publication
- 2011
Drugs