| | | Duplication | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Deletion | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Deletion | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Deletion | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Deletion | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Single nucleotide variant (missense variant) | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Single nucleotide variant (intron variant) | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Microsatellite (frameshift variant) | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Single nucleotide variant (missense variant) | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Single nucleotide variant (intron variant) | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Single nucleotide variant (intron variant) | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Single nucleotide variant (missense variant +2 more) | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Single nucleotide variant (missense variant) | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Single nucleotide variant (missense variant) | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (missense variant) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (intron variant) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (missense variant) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Duplication (inframe_insertion) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (intron variant) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (missense variant +2 more) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (intron variant) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (missense variant) | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Single nucleotide variant (nonsense) | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Single nucleotide variant (missense variant) | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Single nucleotide variant (missense variant) | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Single nucleotide variant (missense variant) | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Single nucleotide variant (missense variant) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (intron variant) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (missense variant +2 more) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (missense variant) | Seizure +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (intron variant) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (missense variant) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (missense variant) | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Single nucleotide variant (intron variant) | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Single nucleotide variant (splice acceptor variant) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (missense variant) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (missense variant) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (intron variant) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (missense variant) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Single nucleotide variant (intron variant) | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (intron variant) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (intron variant) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (intron variant) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (intron variant) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (intron variant) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (intron variant) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (missense variant) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (intron variant) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (missense variant) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (intron variant) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (intron variant) | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Single nucleotide variant (intron variant) | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Single nucleotide variant (intron variant) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (intron variant) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (missense variant) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (intron variant +2 more) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (missense variant) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (intron variant) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Deletion (frameshift variant) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (nonsense) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (missense variant +2 more) | not provided +2 more | |
| | | Deletion | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Duplication | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Deletion | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Deletion | Epilepsy, childhood absence, susceptibility to, 1 +1 more | |
| | | Single nucleotide variant (missense variant) | Epilepsy, childhood absence, susceptibility to, 1 +2 more | |
| | | Single nucleotide variant (missense variant) | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |
| | | Single nucleotide variant (intron variant) | Epilepsy, childhood absence, susceptibility to, 5 +1 more | |