Annotation Detail
Information
- Associated Genes
- MTRR
- Associated Variants
-
MTRR p.Ile22Met (p.I22M)
(
ENST00000264668.6,
ENST00000440940.7 )
MTRR p.Ile22Met (p.I22M) ( ENST00000264668.6, ENST00000440940.7 ) - Associated Disease
- congenital heart defects
- Source Database
- DisGeNET
- Description
- Association between methionine synthase reductase A66G polymorphism and the risk of congenital heart defects: evidence from eight case-control studies.
- Pubmed
- 24913415
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.0159167194958788
- Year of publication
- 2014
Drugs