| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC129931065, PRMT6 (D150E) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129931065, PRMT6 (S168N) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene