| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | CNNM3, LOC129934367 (A202G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CNNM3, LOC129934367 (V211A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CNNM3, LOC129934367 (Q219R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CNNM3, LOC129934367 (A221G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CNNM3, LOC129934367 (G227S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene