| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CACNB4, LOC129934925 (P15R) | Single nucleotide variant (missense variant) | CACNB4-related condition +6 more | GConflicting classifications of pathogenicity |
| | LOC129934925, CACNB4 (S2F) | Single nucleotide variant (missense variant) | Epilepsy, idiopathic generalized, susceptibility to, 9 +6 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene