| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | ANKDD1A, LOC125078104 (E220V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ANKDD1A, LOC125078104 (E220K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ANKDD1A, LOC125078104 (R210Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene