Links from MedGen
Items: 2
| Gene(s) | Protein change | Condition(s) | Clinical significance
(Last reviewed) | Review status |
|---|
| - GRCh37:
- Chr18:46476629
- GRCh38:
- Chr18:48950259
| SMAD7 | G56S | Colorectal cancer, susceptibility to, 3, Inborn genetic diseases | Uncertain significance
(Nov 18, 2022) | criteria provided, multiple submitters, no conflicts |
| - GRCh37:
- Chr18:46453463
- GRCh38:
- Chr18:48927093
| SMAD7 | | Colorectal cancer, susceptibility to, 3 | risk factor
(May 1, 2008) | no assertion criteria provided |