Annotation Detail
Information
- Associated Genes
- MYL2
- Associated Variants
-
MYL2 c.402+245T>C
(
ENST00000713801.1,
ENST00000713803.1,
ENST00000548438.1,
ENST00000663220.1,
ENST00000713831.1,
ENST00000713804.1,
ENST00000713805.1,
ENST00000713800.1,
ENST00000713806.1,
ENST00000713828.1,
ENST00000228841.15,
ENST00000713827.1,
ENST00000713830.1,
ENST00000713829.1,
ENST00000713826.1 )
MYL2 c.402+245T>C ( ENST00000228841.15, ENST00000548438.1, ENST00000663220.1, ENST00000713800.1, ENST00000713801.1, ENST00000713803.1, ENST00000713804.1, ENST00000713805.1, ENST00000713806.1, ENST00000713826.1, ENST00000713827.1, ENST00000713828.1, ENST00000713829.1, ENST00000713830.1, ENST00000713831.1 ) - Associated Disease
- Coronary heart disease
- Source Database
- DisGeNET
- Description
- A genome-wide association study of a coronary artery disease risk variant.
- Pubmed
- 23364394
- Original source reporting the Gene Disease association
- GWASCAT
- DisGENET score for the Gene Disease association
- 0.12
- Year of publication
- 2013
Drugs