| | | Microsatellite (5 prime UTR variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Hyperaldosteronism, familial, type IV +1 more | |
| | | Single nucleotide variant (synonymous variant) | Hyperaldosteronism, familial, type IV +2 more | |
| | | Single nucleotide variant (missense variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (missense variant) | Idiopathic generalized epilepsy +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Hyperaldosteronism, familial, type IV +1 more | |
| | | Single nucleotide variant (synonymous variant) | Hyperaldosteronism, familial, type IV +1 more | |
| | | Single nucleotide variant (missense variant) | Hyperaldosteronism, familial, type IV +1 more | |
| | | Single nucleotide variant (synonymous variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (synonymous variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (synonymous variant) | Hyperaldosteronism, familial, type IV +2 more | |
| | | Single nucleotide variant (missense variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (synonymous variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (missense variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (missense variant) | Idiopathic generalized epilepsy +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Hyperaldosteronism, familial, type IV +1 more | |
| | | Single nucleotide variant (synonymous variant) | Hyperaldosteronism, familial, type IV +2 more | |
| | | Single nucleotide variant (synonymous variant) | Hyperaldosteronism, familial, type IV +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (synonymous variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (missense variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (missense variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (synonymous variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (missense variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (missense variant) | Hyperaldosteronism, familial, type IV +1 more | |
| | | Single nucleotide variant (synonymous variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (synonymous variant) | Hyperaldosteronism, familial, type IV +1 more | |
| | | Single nucleotide variant (missense variant) | Hyperaldosteronism, familial, type IV +3 more | |
| | | Single nucleotide variant (synonymous variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | Idiopathic generalized epilepsy +2 more | |
| | | Single nucleotide variant (missense variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (synonymous variant) | Hyperaldosteronism, familial, type IV +1 more | |
| | | Single nucleotide variant (synonymous variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (missense variant) | Idiopathic generalized epilepsy +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (missense variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (synonymous variant) | Idiopathic generalized epilepsy +2 more | |
| | | Single nucleotide variant (synonymous variant) | Hyperaldosteronism, familial, type IV +1 more | |
| | | Indel (missense variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (synonymous variant) | Hyperaldosteronism, familial, type IV +1 more | |
| | | Single nucleotide variant (missense variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (synonymous variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (synonymous variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (missense variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (synonymous variant) | Idiopathic generalized epilepsy +2 more | |
| | | Single nucleotide variant (synonymous variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (missense variant) | Hyperaldosteronism, familial, type IV +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (missense variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (missense variant) | Epilepsy, childhood absence, susceptibility to, 6 | |
| | | Single nucleotide variant (missense variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (missense variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (synonymous variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (missense variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (synonymous variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (missense variant) | Hyperaldosteronism, familial, type IV +1 more | |
| | | Single nucleotide variant (synonymous variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (missense variant) | Epilepsy, childhood absence, susceptibility to, 6 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Hyperaldosteronism, familial, type IV +1 more | |
| | | Single nucleotide variant (missense variant) | Idiopathic generalized epilepsy +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (missense variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (missense variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (missense variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (synonymous variant) | Hyperaldosteronism, familial, type IV +1 more | |
| | | Single nucleotide variant (synonymous variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (missense variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +3 more | |
| | | Single nucleotide variant (missense variant) | Idiopathic generalized epilepsy +2 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (missense variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (missense variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (missense variant) | Hyperaldosteronism, familial, type IV +2 more | |
| | | Single nucleotide variant (missense variant) | Hyperaldosteronism, familial, type IV +2 more | |
| | | Microsatellite (inframe_deletion) | Epilepsy, childhood absence, susceptibility to, 6 +2 more | |
| | | Single nucleotide variant (synonymous variant) | Hyperaldosteronism, familial, type IV +1 more | |
| | | Single nucleotide variant (missense variant) | Hyperaldosteronism, familial, type IV +1 more | |
| | | Single nucleotide variant (synonymous variant) | Hyperaldosteronism, familial, type IV +1 more | |
| | | Single nucleotide variant (missense variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (synonymous variant) | Hyperaldosteronism, familial, type IV +1 more | |
| | | Single nucleotide variant (missense variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (synonymous variant) | Hyperaldosteronism, familial, type IV +1 more | |
| | | Single nucleotide variant (synonymous variant) | Hyperaldosteronism, familial, type IV +1 more | |
| | | Single nucleotide variant (missense variant) | Idiopathic generalized epilepsy +1 more | |
| | | Single nucleotide variant (missense variant) | Hyperaldosteronism, familial, type IV +1 more | |
| | | Single nucleotide variant (missense variant) | Hyperaldosteronism, familial, type IV +1 more | |
| | | Single nucleotide variant (missense variant) | Hyperaldosteronism, familial, type IV +1 more | |
| | | Single nucleotide variant (synonymous variant) | Hyperaldosteronism, familial, type IV +1 more | |