| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LINC02734, PRCP (H480R +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PRCP, LINC02734 (R355H +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LINC02734, PRCP (V343F +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LINC02734, PRCP (T304A +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LINC02734, PRCP (L226V +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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