Annotation Detail
Information
- Associated Genes
- AKAP9
- Associated Variants
-
AKAP9 MUTATION
AKAP9 MUTATION - Associated Disease
- Congenital long QT syndrome
- Source Database
- DisGeNET
- Description
- AKAP9 is a genetic modifier of congenital long-QT syndrome type 1.
- Pubmed
- 25087618
- Section of the abstract supporting the evidence
- TITLE
- Number of the section of the abstract supporting the evidence
- 0
- Number of the sentence supporting the evidence
- 0
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.000271441872080303
Drugs