| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130062899, STK11 (R331Q) | Single nucleotide variant (missense variant) | Peutz-Jeghers syndrome +3 more | GConflicting classifications of pathogenicity |
| | LOC130062899, STK11 (V338M) | Single nucleotide variant (missense variant) | Peutz-Jeghers syndrome +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant) | Hereditary cancer +6 more | GConflicting classifications of pathogenicity |
| | LOC130062899, STK11 (A347T) | Single nucleotide variant (missense variant) | Peutz-Jeghers syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Hereditary cancer-predisposing syndrome +2 more | |
| | LOC130062899, STK11 (F354L) | Single nucleotide variant (missense variant) | Peutz-Jeghers syndrome +7 more | |
| | LOC130062899, STK11 (T363I) | Single nucleotide variant (missense variant) | Peutz-Jeghers syndrome +2 more | GConflicting classifications of pathogenicity |
| | LOC130062899, STK11 (T367M) | Single nucleotide variant (missense variant) | not specified +3 more | GConflicting classifications of pathogenicity |
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