| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC122094899, WNT2B (A18T) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | WNT2B, LOC122094899 (V22A) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC122094899, WNT2B (P27S) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC122094899, WNT2B (S59C) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
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