| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC129931453, LOC129931454 +1585 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | CADM3, CADM3-AS1 (D194E +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | CADM3, CADM3-AS1 (H197Q +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | CADM3, CADM3-AS1 (R199H +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | CADM3, CADM3-AS1 (A365T +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | CADM3, CADM3-AS1 (G288C +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Charcot-Marie-Tooth disease, axonal, type 2FF | |
| | CADM3, CADM3-AS1 (I349L +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | CADM3, CADM3-AS1 (Y308C +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided +1 more | |
| | CADM3, CADM3-AS1 (H319N +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | CADM3, CADM3-AS1 (A330V +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
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