| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | NTMT1, ASB6 (H128R +1 more) | Single nucleotide variant (3 prime UTR variant +2 more) | Inborn genetic diseases | |
| | NTMT1, ASB6 (R104K +1 more) | Single nucleotide variant (3 prime UTR variant +2 more) | Inborn genetic diseases | |
Click to view in NCBI Gene