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
- Migraine Disorders
- Source Database
- DisGeNET
- Description
- Genotypes of the MTHFR C677T and MTRR A66G genes act independently to reduce migraine disability in response to vitamin supplementation.
- Pubmed
- 22926161
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.000271441872080303
- Year of publication
- 2012
Drugs