| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126806608, WNT7A (E186K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126806608, WNT7A (R157C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126806608, WNT7A (D130E) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126806608, WNT7A (T124I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126806608, WNT7A (I111V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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