| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC125177445, MYO18A (R1844W +4 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC125177445, MYO18A (R1434K +4 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC125177445, MYO18A (A1406T +4 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | MYO18A, LOC125177445 (E1901K +4 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC125177445, MYO18A (E1869V +4 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | sellar metastasis from primary bronchial carcinoid tumor | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Translocation | Atypical chronic myeloid leukemia, BCR-ABL1 negative | |
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