| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | TGFB1-related condition +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | LOC130064510, TGFB1 (S83T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene