| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC129996682, PHF3 (V555M +1 more) | Single nucleotide variant (missense variant +1 more) | PHF3-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | PHF3-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | PHF3-related disorder | |
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