| | | Deletion (frameshift variant +1 more) | Galloway-Mowat syndrome 1 | |
| | | Single nucleotide variant (nonsense +1 more) | Galloway-Mowat syndrome 1 | |
| | | Single nucleotide variant (missense variant +1 more) | Galloway-Mowat syndrome 1 | |
| | | Single nucleotide variant (missense variant +1 more) | Galloway-Mowat syndrome 1 | |
| | | Single nucleotide variant (nonsense +1 more) | Galloway-Mowat syndrome 1 | |
| | | Single nucleotide variant (missense variant +1 more) | Galloway-Mowat syndrome 1 | |
| | | Single nucleotide variant (missense variant +1 more) | Galloway-Mowat syndrome 1 | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Galloway-Mowat syndrome 1 | |
| | | Single nucleotide variant (missense variant +1 more) | Galloway-Mowat syndrome 1 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Galloway-Mowat syndrome 1 | |
| | | Duplication (nonsense +1 more) | Galloway-Mowat syndrome 1 +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant +1 more) | Galloway-Mowat syndrome 1 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Galloway-Mowat syndrome 1 | |
| | | Microsatellite (frameshift variant +1 more) | Galloway-Mowat syndrome 1 | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +2 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Galloway-Mowat syndrome 1 +1 more | |
| | | Microsatellite (inframe_insertion +1 more) | not provided +1 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Galloway-Mowat syndrome 1 +1 more | |
| | | Microsatellite (inframe_deletion +1 more) | not provided +1 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Galloway-Mowat syndrome 1 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (nonsense +1 more) | Galloway-Mowat syndrome 1 +1 more | GPathogenic/Likely pathogenic |
| | | Duplication (frameshift variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Galloway-Mowat syndrome 1 | |
| | | Duplication (frameshift variant +1 more) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Microsatellite (inframe_deletion +1 more) | Galloway-Mowat syndrome 1 +1 more | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Galloway-Mowat syndrome 1 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | WDR73-related condition +2 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Galloway-Mowat syndrome 1 | |
| | | Single nucleotide variant (missense variant +1 more) | Galloway-Mowat syndrome 1 +1 more | |
| | | Single nucleotide variant (missense variant) | Galloway-Mowat syndrome 1 | |
| | | Single nucleotide variant (missense variant) | Galloway-Mowat syndrome 1 | |
| | | Single nucleotide variant (missense variant +1 more) | Galloway-Mowat syndrome 1 +1 more | |
| | | Single nucleotide variant (intron variant) | Galloway-Mowat syndrome 1 +1 more | |
| | | | Abnormality of neuronal migration | |
| | | Duplication (frameshift variant +1 more) | WDR73-related condition +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Galloway-Mowat syndrome 1 | |
| | | Deletion (frameshift variant +1 more) | not provided +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Galloway-Mowat syndrome 1 +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | Galloway-Mowat syndrome 1 | |
| | | Microsatellite (frameshift variant +1 more) | Galloway-Mowat syndrome 1 | |
| | | Single nucleotide variant (nonsense +1 more) | Nephrotic syndrome +1 more | GPathogenic/Likely pathogenic |
| | | Duplication (frameshift variant +1 more) | Galloway-Mowat syndrome 1 +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense +1 more) | Galloway-Mowat syndrome 1 | |
| | | Single nucleotide variant (missense variant +1 more) | Telangiectasia, hereditary hemorrhagic, type 1 | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Galloway-Mowat syndrome 1 | |