1 => The disorder is placed on the map based on its association with a gene, but the underlying defect is not known
2 => The disorder has been placed on the map by linkage; no mutation has been found
3 => The molecular basis for the disorder is known; a mutation has been found in the gene
4 => A contiguous gene deletion or duplication syndrome, multiple genes are deleted or duplicated causing the phenotype
| Gene Symbol | Chromosomal Location | Gene MIM number | Mapping Method | Phenotype | Phenotype MIM number | Phenotype Mapping Key |
| RAF1 | 3p25.2 | 164760 | REa, Fd, A | Noonan syndrome 5, 611553 (3) | 611553 | 3 |
| RAF1 | 3p25.2 | 164760 | REa, Fd, A | LEOPARD syndrome 2, 611554 (3) | 611554 | 3 |
| RAF1 | 3p25.2 | 164760 | REa, Fd, A | Cardiomyopathy, dilated, 1NN, 615916 (3) | 615916 | 3 |