| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (splice donor variant) | Hypertrophic osteoarthropathy, primary, autosomal recessive, 2 | |
| | | Single nucleotide variant (missense variant) | Hypertrophic osteoarthropathy, primary, autosomal recessive, 2 | |
| | LOC123038185, SLCO2A1 (P457L) | Single nucleotide variant (missense variant) | Hypertrophic osteoarthropathy, primary, autosomal recessive, 2 | |
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