| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | KCNQ5, KCNQ5-DT
+1 more (R3S) | Single nucleotide variant (missense variant) | Inborn genetic diseases +2 more | GConflicting classifications of pathogenicity |
| | KCNQ5, KCNQ5-DT
+1 more (G8R) | Single nucleotide variant (missense variant) | KCNQ5-related disorder +2 more | |
Click to view in NCBI Gene