| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant) | KCTD3-related condition | |
| | | Single nucleotide variant (synonymous variant) | KCTD3-related condition | |
| | | Duplication (inframe insertion) | KCTD3-related condition | |
Click to view in NCBI Gene