| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +5 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Seizures, benign familial neonatal, 2 +4 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +4 more | |
| | | Single nucleotide variant (intron variant) | Inborn genetic diseases +3 more | |
| | | Single nucleotide variant (intron variant) | Seizures, benign familial neonatal, 2 +1 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +4 more | |
| | | Indel (missense variant) | Benign neonatal seizures +2 more | |
| | | Single nucleotide variant (intron variant) | Benign neonatal seizures +2 more | |
| | | Single nucleotide variant (missense variant) | Benign neonatal seizures +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Seizures, benign familial neonatal, 2 +2 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +3 more | |
| | | Single nucleotide variant (missense variant) | KCNQ3-related developmental disability +8 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Seizures, benign familial neonatal, 2 +1 more | |