| | | Single nucleotide variant (stop lost) | not provided | |
| | | Single nucleotide variant (nonsense +1 more) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Deletion (frameshift variant) | Dilated cardiomyopathy 1GG | |
| | | Deletion (frameshift variant) | Dilated cardiomyopathy 1GG | |
| | | Duplication (frameshift variant) | Dilated cardiomyopathy 1GG | |
| | | Single nucleotide variant (splice donor variant) | Dilated cardiomyopathy 1GG | |
| | | Single nucleotide variant (intron variant) | Dilated cardiomyopathy 1GG | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1GG | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1GG | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1GG | |
| | | Single nucleotide variant (intron variant) | Dilated cardiomyopathy 1GG | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1GG | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1GG | |
| | | Deletion (nonsense) | Dilated cardiomyopathy 1GG | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1GG | |
| | | Microsatellite (frameshift variant) | Dilated cardiomyopathy 1GG | |
| | | Single nucleotide variant (missense variant +1 more) | Dilated cardiomyopathy 1GG | |
| | | Duplication (frameshift variant) | Dilated cardiomyopathy 1GG | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1GG | |
| | | Deletion | Paragangliomas 5 | |
| | | Deletion | Familial cancer of breast | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Duplication | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Copy number loss | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number loss | not provided | |
| | | Deletion (splice acceptor variant +1 more) | Paragangliomas 5 | |
| | | Duplication | Paragangliomas 5 +1 more | |
| | | Duplication | Mitochondrial complex II deficiency, nuclear type 1 +1 more | |