| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Familial hyperaldosteronism type II | |
| | | Single nucleotide variant (nonsense) | Familial hyperaldosteronism type II | |
| | | Single nucleotide variant (missense variant) | Epilepsy, idiopathic generalized, susceptibility to, 11 +2 more | |
| | | Single nucleotide variant (missense variant) | Familial hyperaldosteronism type II | |
| | | Single nucleotide variant (missense variant) | Familial hyperaldosteronism type II | |
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