| | | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Auriculocondylar syndrome 2 +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (intron variant) | Auriculocondylar syndrome 2 | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Auriculocondylar syndrome 2 | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Malignant tumor of prostate | |
| | | Single nucleotide variant (missense variant) | Auriculocondylar syndrome 2 | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Auriculocondylar syndrome 2 +1 more | |
| | | Duplication (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Auriculocondylar syndrome 2 | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Auriculocondylar syndrome 2 | |
| | | Single nucleotide variant (synonymous variant) | PLCB4-related disorder | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Auriculocondylar syndrome 2 | |
| | | Single nucleotide variant (missense variant) | Auriculocondylar syndrome 2 +1 more | |
| | | Single nucleotide variant (intron variant) | Auriculocondylar syndrome 2 | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | Auriculocondylar syndrome 2 | |
| | | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Auriculocondylar syndrome 2 +1 more | |
| | | Single nucleotide variant (intron variant) | Auriculocondylar syndrome 2 | |
| | | Single nucleotide variant (intron variant) | Auriculocondylar syndrome 2 | |
| | | Single nucleotide variant (synonymous variant) | Auriculocondylar syndrome 2 | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Auriculocondylar syndrome 2 | |
| | | Single nucleotide variant (missense variant) | Auriculocondylar syndrome 2 | |
| | | Single nucleotide variant (missense variant) | Auriculocondylar syndrome 1 | |
| | | Single nucleotide variant (missense variant) | Auriculocondylar syndrome 2 | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Auriculocondylar syndrome 2 | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Auriculocondylar syndrome 2 +1 more | |
| | | Single nucleotide variant (missense variant) | Auriculocondylar syndrome 2 | |
| | | Single nucleotide variant (missense variant) | Auriculocondylar syndrome 2 | |
| | | Single nucleotide variant (missense variant) | Auriculocondylar syndrome 2 | |
| | | Single nucleotide variant (missense variant) | Auriculocondylar syndrome 2 | |
| | | Single nucleotide variant (missense variant) | PLCB4-related disorder | |
| | | Duplication (intron variant) | not provided | |
| | | Duplication (intron variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Auriculocondylar syndrome 2 | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | PLCB4-related disorder | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Auriculocondylar syndrome 2 | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Auriculocondylar syndrome 2 | |
| | | Single nucleotide variant (synonymous variant) | Auriculocondylar syndrome 2 +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | PLCB4-related disorder | |
| | | Single nucleotide variant (intron variant) | Auriculocondylar syndrome 2 +1 more | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Deletion (splice acceptor variant +1 more) | Auriculocondylar syndrome 2 | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Auriculocondylar syndrome 2 | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Microsatellite (inframe_deletion) | not specified | |
| | | Single nucleotide variant (synonymous variant) | Auriculocondylar syndrome 2 | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Insertion (intron variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Auriculocondylar syndrome 2 | |
| | | Single nucleotide variant (intron variant) | Auriculocondylar syndrome 2 | |
| | | 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 provided | |
| | | Single nucleotide variant (intron variant) | Auriculocondylar syndrome 2 | |