| | | Deletion (intron variant) | Familial atrial myxoma +3 more | |
| | | Duplication (intron variant) | Carney complex, type 1 +4 more | |
| | | Single nucleotide variant (intron variant) | Familial atrial myxoma +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial atrial myxoma +3 more | |
| | | Single nucleotide variant (missense variant) | Carney complex, type 1 +3 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +4 more | |
| | | Microsatellite (inframe_deletion) | Carney complex, type 1 +3 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +5 more | |
| | | Single nucleotide variant (missense variant) | Carney complex, type 1 +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | Carney complex, type 1 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Carney complex, type 1 +4 more | |
| | | Single nucleotide variant (synonymous variant) | Carney complex, type 1 +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | Acrodysostosis 1 with or without hormone resistance +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Hereditary cancer-predisposing syndrome +6 more | |
| | | Single nucleotide variant (nonsense +1 more) | not provided +3 more | |
| | | Microsatellite (splice acceptor variant) | Carney complex, type 1 +3 more | |
| | | Deletion | Pigmented nodular adrenocortical disease, primary, 1 | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | Carney complex, type 1 | |