FANCC
HGNC:3584 · SaudiVarKB evidence summary derived from retained literature mentions.
3Gene mentions
3Publications
1Linked variants
3Associated phenotypes
Associated phenotypes
Co-mentioned in FANCC publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| leukemia | — | 1 | 1 |
| ovarian cancer | — | 1 | 1 |
| breast cancer | — | 1 | 1 |
Linked variants
Variants normalized to FANCC| Variant | HGVS / rsID | Articles | Mentions |
|---|---|---|---|
| p.Leu492Pro | p.Leu492Pro | 1 | 1 |
Population context
Reported in the same publications| Country / region | Group | Cohort | Articles |
|---|---|---|---|
| Not specified | — | 15 | 1 |
| Saudi Arabia | — | 2,015 | 1 |
| Not specified | — | 147 | 1 |
Supporting publications
3 records- 2023Genetic analyses of DNA repair pathway associated genes implicate new candidate cancer predisposing genes in ancestrally defined ovarian cancer cases.Frontiers in oncologyPubMed ↗
- 2022Germline predisposition to pediatric Ewing sarcoma is characterized by inherited pathogenic variants in DNA damage repair genes.American journal of human geneticsPubMed ↗
- 2016Clinical characteristics and genetic subtypes of Fanconi anemia in Saudi patients.Cancer geneticsPubMed ↗