Annotation Detail
Information
- Associated Genes
- FANCG
- Associated Variants
-
FANCG MUTATION
FANCG MUTATION - Associated Disease
- FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
- Source Database
- DisGeNET
- Description
- Founder haplotype analysis of Fanconi anemia in the Korean population finds common ancestral haplotypes for a FANCG variant.
- Pubmed
- 25703136
- 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
- 0.00651460492992728
Drugs