| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +4 more | |
| | | Single nucleotide variant (intron variant) | not specified +4 more | |
| | | Single nucleotide variant (missense variant) | Peutz-Jeghers syndrome +2 more | GConflicting classifications of pathogenicity |
| | LOC130062899, STK11 (V338M) | Single nucleotide variant (missense variant) | Carcinoma of pancreas +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Peutz-Jeghers syndrome +4 more | |
Click to view in NCBI Gene