| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Congenital prothrombin deficiency +1 more | |
| | | Single nucleotide variant | not provided +4 more | GPathogenic/Likely pathogenic/Pathogenic, low penetrance; risk factor |
Click to view in NCBI Gene