| | | Single nucleotide variant (missense variant +1 more) | Epilepsy, idiopathic generalized, susceptibility to, 9 | |
| | | Single nucleotide variant (missense variant) | Epilepsy, idiopathic generalized, susceptibility to, 9 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Epilepsy, idiopathic generalized, susceptibility to, 9 | |
| | | Single nucleotide variant (intron variant) | Epilepsy, idiopathic generalized, susceptibility to, 9 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Episodic ataxia type 5 +2 more | |
| | | Single nucleotide variant (missense variant) | Idiopathic generalized epilepsy +3 more | |
| | | Single nucleotide variant (missense variant) | Epilepsy, idiopathic generalized, susceptibility to, 9 +2 more | |
| | | Deletion (frameshift variant +1 more) | Epilepsy, idiopathic generalized, susceptibility to, 9 | |
| | | Single nucleotide variant (missense variant +1 more) | Epilepsy, idiopathic generalized, susceptibility to, 9 +2 more | |
| | CACNB4, LOC129934925 (P15R) | Single nucleotide variant (missense variant) | Episodic ataxia type 5 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | CACNB4, LOC129934925 (S2F) | Single nucleotide variant (missense variant) | Episodic ataxia type 5 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not provided +3 more | GConflicting classifications of pathogenicity |