| | | Single nucleotide variant (intron variant) | SDHD-related condition | |
| | | Single nucleotide variant (intron variant) | SDHD-related condition | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | SDHD-related condition | |
| | | Single nucleotide variant (synonymous variant +1 more) | SDHD-related condition | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | Carney-Stratakis syndrome +3 more | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (missense variant +3 more) | Pheochromocytoma +3 more | |
| | | Duplication (intron variant) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (intron variant) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (intron variant) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (intron variant) | Pheochromocytoma +3 more | |
| | | Indel (missense variant +2 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (splice acceptor variant +1 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Pheochromocytoma +3 more | |
| | | Duplication (frameshift variant +2 more) | Pheochromocytoma +3 more | |
| | | Indel (missense variant +2 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (nonsense +2 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (intron variant) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (intron variant) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (intron variant) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (intron variant) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | Pheochromocytoma +3 more | |
| | | Microsatellite (intron variant) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (intron variant) | Pheochromocytoma +3 more | |
| | | Microsatellite (intron variant) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (intron variant) | Paragangliomas with sensorineural hearing loss +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Paragangliomas with sensorineural hearing loss +3 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Paragangliomas with sensorineural hearing loss +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (intron variant) | Paragangliomas with sensorineural hearing loss +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (intron variant) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (intron variant) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (intron variant) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Pheochromocytoma +3 more | |
| | | Deletion (frameshift variant +2 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (intron variant) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (nonsense +2 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (intron variant) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Pheochromocytoma +3 more | |
| | | Deletion (frameshift variant +1 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (missense variant +3 more) | Pheochromocytoma +3 more | |
| | | Single nucleotide variant (missense variant +2 more) | Pheochromocytoma +3 more | |
| | | Copy number gain | not provided | |
| | | Duplication (frameshift variant +2 more) | not provided | |
| | | Single nucleotide variant (missense variant +2 more) | Mitochondrial complex 2 deficiency, nuclear type 3 | |
| | | Single nucleotide variant (nonsense +3 more) | Mitochondrial complex 2 deficiency, nuclear type 3 | |
| | | Single nucleotide variant (missense variant +3 more) | Paragangliomas 1 | |
| | | Duplication | not provided | |
| | | Single nucleotide variant (nonsense +2 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Indel (nonsense +2 more) | Pheochromocytoma | |
| | | Single nucleotide variant (missense variant +1 more) | SDHD-related condition | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (synonymous variant +2 more) | Hereditary cancer-predisposing syndrome +4 more | |
| | | Single nucleotide variant (missense variant +2 more) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (missense variant +2 more) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | Hereditary cancer-predisposing syndrome +4 more | |
| | | Single nucleotide variant (synonymous variant +3 more) | not provided +4 more | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | not provided | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | Carney-Stratakis syndrome +4 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified | |
| | | Single nucleotide variant (splice acceptor variant +1 more) | not provided | |
| | | Deletion (frameshift variant +2 more) | not provided | |
| | | Deletion (non-coding transcript variant +2 more) | Paragangliomas 1 | |
| | | Single nucleotide variant (missense variant +2 more) | not provided | |
| | | Deletion (frameshift variant +2 more) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (missense variant +2 more) | Hereditary cancer-predisposing syndrome +4 more | |
| | | Deletion (frameshift variant +2 more) | Hereditary cancer-predisposing syndrome | |