| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | KCTD13, LOC130058798 (E25D) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | KCTD13, LOC130058798 (E25Q) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | KCTD13, LOC130058798 (E17K) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene