| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant +1 more) | Idiopathic generalized epilepsy +2 more | |
| | | Single nucleotide variant (missense variant) | not specified +4 more | |
| | LOC129934925, CACNB4 (P15R) | Single nucleotide variant (missense variant) | CACNB4-related disorder +6 more | GConflicting classifications of pathogenicity |
| | CACNB4, LOC129934925 (S2F) | Single nucleotide variant (missense variant) | Epilepsy, idiopathic generalized, susceptibility to, 9 +6 more | GConflicting classifications of pathogenicity |
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