| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | 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-AS1, CADM3 (A365T +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | CADM3, CADM3-AS1 (H319N +2 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
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