| | | Microsatellite (non-coding transcript variant +1 more) | Cataract 30 | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Cataract 30 | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | VIM-related condition | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | LOC130003452, VIM +1 more (V77M) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Cataract 30 | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Cataract 30 | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Cataract 30 | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Cataract 30 | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | Cataract 30 | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Cataract 30 | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | VIM-related condition +1 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | VIM-related condition +1 more | |
| | LOC130003452, VIM +1 more (S56Y) | Single nucleotide variant (non-coding transcript variant +1 more) | Cataract 30 | |
| | | Deletion (non-coding transcript variant +1 more) | Cataract 30 +1 more | GPathogenic/Likely pathogenic |
| | LOC130003185, LOC130003186 +680 more | Copy number loss | See cases | |
| | CUBN, LOC111501766 +23 more | Copy number gain | See cases | |
| | LOC130003254, LOC130003255 +1221 more | Copy number gain | See cases | |
| | LINC00700, LINC00701 +837 more | Copy number gain | See cases | |
| | ACBD7, ACBD7-DCLRE1CP1 +388 more | Copy number loss | See cases | |
| | LOC126860819, LOC126860820 +680 more | Copy number gain | See cases | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Cataract 30 | |