| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | CCDC6, LOC130003860 (G32S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CCDC6, LOC130003860 (G14W) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CCDC6, LOC130003860 (A13T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene