| | GIT1, TP53I13 (A707T +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | GIT1, TP53I13 (G612W +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | GIT1, TP53I13 (D597A +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | GIT1, TP53I13 (T584M +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TP53I13, GIT1 (R555W +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | GIT1, TP53I13 (A488V +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | GIT1, TP53I13 (A497T +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | GIT1, TP53I13 (L492F +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TP53I13, GIT1 (R455Q +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TP53I13, GIT1 (S423L +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TP53I13, GIT1 (R409Q +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | GIT1, TP53I13 (I356V +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TP53I13, GIT1 (A320V +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |