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 |
| TP53 | 17p13.1 | 191170 | REa, A, D | Colorectal cancer, 114500 (3) | 114500 | 3 |
| TP53 | 17p13.1 | 191170 | REa, A, D | Li-Fraumeni syndrome, 151623 (3) | 151623 | 3 |
| TP53 | 17p13.1 | 191170 | REa, A, D | Hepatocellular carcinoma, 114550 (3) | 114550 | 3 |
| TP53 | 17p13.1 | 191170 | REa, A, D | Osteosarcoma, 259500 (3) | 259500 | 3 |
| TP53 | 17p13.1 | 191170 | REa, A, D | Choroid plexus papilloma, 260500 (3) | 260500 | 3 |
| TP53 | 17p13.1 | 191170 | REa, A, D | Nasopharyngeal carcinoma, 607107 (3) | 607107 | 3 |
| TP53 | 17p13.1 | 191170 | REa, A, D | Pancreatic cancer, 260350 (3) | 260350 | 3 |
| TP53 | 17p13.1 | 191170 | REa, A, D | Adrenal cortical carcinoma, 202300 (3) | 202300 | 3 |
| TP53 | 17p13.1 | 191170 | REa, A, D | Breast cancer, 114480 (3) | 114480 | 3 |
| TP53 | 17p13.1 | 191170 | REa, A, D | {Basal cell carcinoma 7}, 614740 (3) | 614740 | 3 |
| TP53 | 17p13.1 | 191170 | REa, A, D | {Glioma susceptibility 1}, 137800 (3) | 137800 | 3 |