| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | ADAR, LOC126805874 (I625L +5 more) | Single nucleotide variant (missense variant) | Symmetrical dyschromatosis of extremities +2 more | |
| | ADAR, LOC126805874 (V858I +5 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +2 more | |
| | ADAR, LOC126805874 (I578M +5 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADAR, LOC126805874 (R850W +5 more) | Single nucleotide variant (missense variant) | Symmetrical dyschromatosis of extremities +2 more | |
Click to view in NCBI Gene