| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | DYNC1H1, LOC126862060 (C2985S) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | Inborn genetic diseases +2 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene