| | | Deletion | Seizures, benign familial neonatal, 1 | |
| | | Deletion | Seizures, benign familial neonatal, 1 | |
| | | Deletion | Seizures, benign familial neonatal, 1 | |
| | | Single nucleotide variant (missense variant) | Early infantile epileptic encephalopathy with suppression bursts +3 more | |
| | | Microsatellite (frameshift variant) | Seizures, benign familial neonatal, 1 | |
| | | Microsatellite (frameshift variant) | Inborn genetic diseases +1 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Early infantile epileptic encephalopathy with suppression bursts +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +5 more | |
| | | Duplication (frameshift variant) | Seizures, benign familial neonatal, 1 | |
| | | Deletion (frameshift variant) | not provided +2 more | |
| | | Deletion (frameshift variant) | Seizures, benign familial neonatal, 1 | |
| | | Single nucleotide variant (synonymous variant) | Early infantile epileptic encephalopathy with suppression bursts | |
| | | Deletion (frameshift variant) | Early infantile epileptic encephalopathy with suppression bursts | |
| | | Deletion (frameshift variant) | Seizures, benign familial neonatal, 1 | |
| | | Single nucleotide variant (missense variant) | Seizures, benign familial neonatal, 1 +1 more | |
| | | Single nucleotide variant (intron variant) | Early infantile epileptic encephalopathy with suppression bursts +1 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant) | Seizures, benign familial neonatal, 1 | |
| | | Single nucleotide variant (missense variant) | Early infantile epileptic encephalopathy with suppression bursts +1 more | |
| | | Single nucleotide variant (missense variant) | Benign Rolandic epilepsy | |
| | | Single nucleotide variant (missense variant) | Seizures, benign familial neonatal, 1 +1 more | |
| | | Single nucleotide variant (splice acceptor variant) | Seizures, benign familial neonatal, 1 | |
| | | Single nucleotide variant (intron variant) | Early infantile epileptic encephalopathy with suppression bursts | |
| | | Deletion | Seizures, benign familial neonatal, 1 | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Early infantile epileptic encephalopathy with suppression bursts +1 more | |
| | | Single nucleotide variant (nonsense) | KCNQ2-related disorder +4 more | |
| | | Indel (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Early infantile epileptic encephalopathy with suppression bursts +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Developmental and epileptic encephalopathy, 7 | |
| | | Single nucleotide variant (synonymous variant) | Inborn genetic diseases +3 more | |
| | | Single nucleotide variant (missense variant) | Early infantile epileptic encephalopathy with suppression bursts +4 more | |
| | | Duplication (frameshift variant) | Seizures, benign familial neonatal, 1 | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Early infantile epileptic encephalopathy with suppression bursts | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Early infantile epileptic encephalopathy with suppression bursts +1 more | |
| | | Single nucleotide variant (missense variant) | Early infantile epileptic encephalopathy with suppression bursts +4 more | |
| | | Single nucleotide variant (missense variant) | Developmental and epileptic encephalopathy, 7 | |
| | | Single nucleotide variant (missense variant) | Early infantile epileptic encephalopathy with suppression bursts +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (splice acceptor variant) | Seizures, benign familial neonatal, 1 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice donor variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Early infantile epileptic encephalopathy with suppression bursts | |
| | | Single nucleotide variant (nonsense) | Seizures, benign familial neonatal, 1 | |
| | | Single nucleotide variant (synonymous variant) | Inborn genetic diseases +2 more | |
| | | Deletion (frameshift variant) | Seizures, benign familial neonatal, 1 | |
| | | Single nucleotide variant (splice donor variant) | Seizures, benign familial neonatal, 1 +1 more | |
| | | Single nucleotide variant (missense variant) | Developmental and epileptic encephalopathy, 7 | |
| | | Deletion (frameshift variant) | Seizures, benign familial neonatal, 1 | |
| | | Single nucleotide variant (missense variant) | Early infantile epileptic encephalopathy with suppression bursts +1 more | |
| | | Single nucleotide variant (nonsense) | not provided +5 more | |
| | | Single nucleotide variant (splice acceptor variant +1 more) | Seizures, benign familial neonatal, 1 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Seizures, benign familial neonatal, 1 | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +2 more | |
| | | Single nucleotide variant (splice donor variant) | Early infantile epileptic encephalopathy with suppression bursts | |
| | | Microsatellite (inframe_deletion) | Seizures, benign familial neonatal, 1 | |
| | | Single nucleotide variant (splice donor variant) | Seizures, benign familial neonatal, 1 | |
| | | Single nucleotide variant (synonymous variant) | Early infantile epileptic encephalopathy with suppression bursts | |
| | | Microsatellite (nonsense) | Seizures, benign familial neonatal, 1 | |
| | | Deletion (frameshift variant) | Early infantile epileptic encephalopathy with suppression bursts +1 more | |
| | | Single nucleotide variant (intron variant +1 more) | Seizures, benign familial neonatal, 1 | |
| | | Deletion (frameshift variant +1 more) | Seizures, benign familial neonatal, 1 | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Seizures, benign familial neonatal, 1 | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Early infantile epileptic encephalopathy with suppression bursts | |
| | | Single nucleotide variant (missense variant) | Seizures, benign familial neonatal, 1 | |
| | | Single nucleotide variant (missense variant) | Developmental and epileptic encephalopathy, 7 | |
| | | Single nucleotide variant (missense variant) | Early infantile epileptic encephalopathy with suppression bursts +1 more | |
| | | Single nucleotide variant (missense variant) | Early infantile epileptic encephalopathy with suppression bursts | |
| | | Single nucleotide variant (missense variant) | Seizures, benign familial neonatal, 1 | |
| | | Single nucleotide variant (synonymous variant) | Early infantile epileptic encephalopathy with suppression bursts | |
| | | Single nucleotide variant (missense variant) | Early infantile epileptic encephalopathy with suppression bursts | |
| | | Single nucleotide variant (missense variant) | Epilepsy, benign neonatal, 1, and/or myokymia | |
| | | Single nucleotide variant (missense variant) | Early infantile epileptic encephalopathy with suppression bursts | |
| | | Single nucleotide variant (splice acceptor variant) | Developmental and epileptic encephalopathy, 7 | |
| | | Single nucleotide variant (missense variant) | Seizure | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Early infantile epileptic encephalopathy with suppression bursts +2 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Developmental and epileptic encephalopathy, 7 | |
| | | Single nucleotide variant (nonsense) | Seizures, benign familial neonatal, 1 | |
| | | Single nucleotide variant (missense variant) | Developmental and epileptic encephalopathy, 7 | |
| | | Duplication (frameshift variant) | Seizures, benign familial neonatal, 2 | |
| | | Single nucleotide variant (splice acceptor variant) | Seizures, benign familial neonatal, 1 | |
| | | Single nucleotide variant (missense variant) | Early infantile epileptic encephalopathy with suppression bursts +1 more | |
| | | Single nucleotide variant (missense variant) | KCNQ2-related disorder +5 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Microsatellite (inframe_deletion) | Seizures, benign familial neonatal, 1 +6 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Developmental and epileptic encephalopathy, 7 +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Epileptic encephalopathy +3 more | |
| | | Single nucleotide variant (missense variant) | Seizure | |
| | | Single nucleotide variant (missense variant) | not provided +5 more | |
| | | Single nucleotide variant (missense variant) | Complex neurodevelopmental disorder +1 more | |