| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CENPF, LOC126806006 (Q116E) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Stromme syndrome | |
| | | Single nucleotide variant (missense variant) | CENPF-related condition +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Stromme syndrome | |
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