| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | IGSF10, MED12L (N2130K +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | IGSF10, MED12L (H2179Q +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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