| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CNNM2, LOC130004628 (D144N) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CNNM2, LOC130004628 (R153H) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene