| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | DIP2C, LOC126860806 (P818S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | DIP2C, LOC126860806 (R774K) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | DIP2C, LOC126860806 (P766T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene