Annotation Detail
Information
- Associated Genes
- RAD51B
- Associated Variants
-
RAD51B c.757-81109G>C
(
ENST00000471583.6,
ENST00000488612.5,
ENST00000487861.5,
ENST00000460526.6,
ENST00000487270.5 )
RAD51B c.757-65951C>T ( ENST00000487270.5, ENST00000487861.5, ENST00000488612.5, ENST00000460526.6, ENST00000471583.6 )
RAD51B c.757-59007C>T ( ENST00000460526.6, ENST00000488612.5, ENST00000487861.5, ENST00000471583.6, ENST00000487270.5 )
RAD51B c.757-81109G>C ( ENST00000460526.6, ENST00000471583.6, ENST00000487270.5, ENST00000487861.5, ENST00000488612.5 )
RAD51B c.757-65951C>T ( ENST00000460526.6, ENST00000471583.6, ENST00000487270.5, ENST00000487861.5, ENST00000488612.5 )
RAD51B c.757-59007C>T ( ENST00000460526.6, ENST00000471583.6, ENST00000487270.5, ENST00000487861.5, ENST00000488612.5 ) - Associated Disease
- atrial fibrillation
- Source Database
- DisGeNET
- Description
- [No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated ]
- Pubmed
- 17903304
- Original source reporting the Gene Disease association
- GAD
- DisGENET score for the Gene Disease association
- 0.00236703197860203
- Year of publication
- 2007
Drugs