| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130064928, PRRG2 (P170S +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130064928, PRRG2 (P171S +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130064928, PRRG2 (P171A +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130064928, PRRG2 (P194L +1 more) | Single nucleotide variant (missense variant) | not specified | |
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