| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC105375218, ZNRF2 (G29R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105375218, LOC129998187 +1 more (A61D) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105375218, ZNRF2 (S89T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105375218, ZNRF2 (A96E) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNRF2, LOC105375218 (P100T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105375218, ZNRF2 (S102G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNRF2, LOC105375218 (P110Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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