| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (3 prime UTR variant) | Melanoma, cutaneous malignant, susceptibility to, 3 | |
| | | Single nucleotide variant (missense variant +1 more) | Familial melanoma +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +3 more | |
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