| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130000699, RMDN1 (P24L) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC130000699, RMDN1 (R22C) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC130000699, RMDN1 (G16V) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
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