| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome | |
| | LOC130062899, STK11 (F354L) | Single nucleotide variant (missense variant) | Melanoma, cutaneous malignant, susceptibility to, 1 +7 more | |
| | LOC130062899, STK11 (D358N) | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +1 more | |
| | LOC130062899, STK11 (T363I) | Single nucleotide variant (missense variant) | Peutz-Jeghers syndrome +2 more | GConflicting classifications of pathogenicity |
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