| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | FZD5, LOC129935506 (R532P) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FZD5, LOC129935506 (H545Y) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
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