| | | Single nucleotide variant (missense variant +1 more) | Atrial fibrillation, familial, 7 | |
| | | Single nucleotide variant (missense variant) | Atrial fibrillation, familial, 7 | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant) | KCNA5-related condition +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Atrial fibrillation, familial, 7 | |
| | | Single nucleotide variant (missense variant) | Atrial fibrillation, familial, 7 | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Atrial fibrillation, familial, 7 +1 more | |
| | | Single nucleotide variant (missense variant) | Atrial fibrillation, familial, 7 +1 more | |
| | | Deletion (inframe_deletion) | Atrial fibrillation, familial, 7 | |
| | | Indel (missense variant) | Atrial fibrillation, familial, 7 | |
| | | Single nucleotide variant (missense variant) | Atrial fibrillation, familial, 7 +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Atrial fibrillation, familial, 7 | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Atrial fibrillation, familial, 7 | |
| | | Indel (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Atrial fibrillation, familial, 7 | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Atrial fibrillation, familial, 7 | |
| | | Single nucleotide variant (missense variant) | Atrial fibrillation, familial, 7 | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant) | Atrial fibrillation, familial, 7 | |
| | | Single nucleotide variant (nonsense) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Atrial fibrillation, familial, 7 | |
| | | Single nucleotide variant (missense variant) | Atrial fibrillation, familial, 7 +1 more | |
| | | Single nucleotide variant (missense variant) | Atrial fibrillation, familial, 7 | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Atrial fibrillation, familial, 7 | |
| | | Single nucleotide variant (missense variant) | Atrial fibrillation, familial, 7 | |
| | | Duplication (frameshift variant) | Atrial fibrillation, familial, 7 +1 more | |
| | | Single nucleotide variant (missense variant) | Atrial fibrillation, familial, 7 | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Atrial fibrillation, familial, 7 | |
| | | Single nucleotide variant (missense variant) | Atrial fibrillation, familial, 7 | |
| | | Single nucleotide variant (missense variant) | Atrial fibrillation, familial, 7 | |
| | | Single nucleotide variant (3 prime UTR variant) | Atrial fibrillation, familial, 7 | |
| | | Single nucleotide variant (3 prime UTR variant) | Atrial fibrillation, familial, 7 | |