Annotation Detail
Information
- Associated Genes
- RAF1
- Associated Variants
-
RAF1 MUTATION
RAF1 MUTATION - Associated Disease
- Noonan syndrome
- Source Database
- DisGeNET
- Description
- Identification of a novel de novo deletion in RAF1 associated with biventricular hypertrophy in Noonan syndrome.
- Pubmed
- 24782337
- 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,CLINVAR,CTD_human,GAD,LHGDN,ORPHANET
- DisGENET score for the Gene Disease association
- 0.383884341699657
Drugs