| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | C21orf62, C21orf62-AS1 (R126S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | C21orf62, C21orf62-AS1 (S148G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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