| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | CDKN2D, LOC130063517 (D20N) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | CDKN2D, LOC130063517 (E4K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene