| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126862606, TRIM37 (D926Y +6 more) | Single nucleotide variant (missense variant +2 more) | Mulibrey nanism syndrome | |
| | | Single nucleotide variant (synonymous variant +2 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | LOC126862606, TRIM37 (E671K +6 more) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases +1 more | |
Click to view in NCBI Gene