| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC107832851, SIRT1 (S14P) | Single nucleotide variant (missense variant) | SIRT1-related disorder +1 more | GConflicting classifications of pathogenicity |
| | LOC107832851, SIRT1 (P37L) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Deletion (inframe_deletion) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | SIRT1-related disorder | |
| | LOC107832851, SIRT1 (A97E) | Single nucleotide variant (missense variant) | SIRT1-related disorder +1 more | |
Click to view in NCBI Gene