| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Copy number gain | not specified | |
| | | Single nucleotide variant | DBH-related condition | |
| | | Single nucleotide variant (intron variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (synonymous variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (synonymous variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (intron variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (synonymous variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (intron variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (intron variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (missense variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (intron variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (synonymous variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (missense variant) | Orthostatic hypotension 1 | |
| | | Duplication (inframe_insertion) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (intron variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (intron variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (intron variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (synonymous variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (synonymous variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (synonymous variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (synonymous variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (intron variant) | Orthostatic hypotension 1 | |
| | | Deletion (frameshift variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (synonymous variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (synonymous variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (synonymous variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (synonymous variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (intron variant +1 more) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (intron variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (synonymous variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (intron variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (missense variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (synonymous variant) | Orthostatic hypotension 1 | |
| | | Deletion (frameshift variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (synonymous variant) | Orthostatic hypotension 1 | |
| | | Microsatellite (frameshift variant) | Orthostatic hypotension 1 | |
| | | Microsatellite (intron variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (intron variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (intron variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (intron variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (synonymous variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (intron variant) | Orthostatic hypotension 1 | |
| | | Copy number gain | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Duplication | Kleefstra syndrome 1 | |
| | | Duplication | Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome | |
| | | Duplication | Orthostatic hypotension 1 | |
| | | Duplication | Orthostatic hypotension 1 | |
| | | Deletion | Orthostatic hypotension 1 | |
| | | Duplication | Rafiq syndrome +4 more | |
| | | Single nucleotide variant (intron variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (synonymous variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Orthostatic hypotension 1 +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Deletion (inframe_deletion) | Inborn genetic diseases | |
| | | Single nucleotide variant (nonsense) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Duplication (intron variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (intron variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (synonymous variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (missense variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (intron variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (missense variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (synonymous variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (missense variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (missense variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (missense variant) | Orthostatic hypotension 1 | |
| | | Single nucleotide variant (intron variant) | Orthostatic hypotension 1 | |