| | | Single nucleotide variant (missense variant) | Thrombophilia due to thrombin defect | |
| | | Single nucleotide variant (missense variant) | Thrombophilia due to thrombin defect | |
| | | Indel (missense variant) | Thrombophilia due to thrombin defect | |
| | | Single nucleotide variant (intron variant) | Thrombophilia due to thrombin defect +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Homocystinuria due to methylene tetrahydrofolate reductase deficiency +3 more | |
| | | Single nucleotide variant (missense variant) | Schizophrenia +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Neural tube defects, folate-sensitive +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Thrombophilia due to thrombin defect +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Thrombophilia due to thrombin defect +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Factor XIII, A subunit, deficiency of +2 more | |
| | | Single nucleotide variant (intron variant) | Congenital prothrombin deficiency +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant | Thrombophilia due to thrombin defect +1 more | |
| | | Single nucleotide variant (missense variant) | Thrombophilia due to thrombin defect +1 more | |
| | | Single nucleotide variant (synonymous variant) | Inborn genetic diseases +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Thrombophilia due to thrombin defect +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +2 more | |
| | | Single nucleotide variant (missense variant) | HABP2-related disorder +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Thrombophilia due to thrombin defect +1 more | |
| | | Single nucleotide variant (intron variant) | Congenital prothrombin deficiency +1 more | |
| | | Single nucleotide variant (missense variant) | Thrombophilia due to thrombin defect +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Thrombophilia due to thrombin defect +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Inborn genetic diseases +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Budd-Chiari syndrome +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Budd-Chiari syndrome +2 more | |
| | | Single nucleotide variant (intron variant) | Thrombophilia due to thrombin defect +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Budd-Chiari syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Budd-Chiari syndrome +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Budd-Chiari syndrome +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Factor V deficiency +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Budd-Chiari syndrome +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Budd-Chiari syndrome +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Budd-Chiari syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant) | Factor V deficiency +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Factor V deficiency +6 more | |
| | | Single nucleotide variant (missense variant) | Budd-Chiari syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | Budd-Chiari syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant) | Budd-Chiari syndrome +3 more | |
| | | Single nucleotide variant (missense variant) | Budd-Chiari syndrome +3 more | |
| | | Single nucleotide variant (missense variant) | Factor V deficiency +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Factor V deficiency +3 more | |
| | | Single nucleotide variant (missense variant) | Factor V deficiency +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Factor V deficiency +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Thrombophilia due to thrombin defect +3 more | |
| | | Single nucleotide variant (missense variant) | Congenital factor V deficiency +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Budd-Chiari syndrome +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Thrombophilia due to thrombin defect +3 more | |
| | | Single nucleotide variant (missense variant) | Thrombophilia due to thrombin defect +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Budd-Chiari syndrome +3 more | |
| | | Single nucleotide variant (missense variant) | Thrombophilia due to thrombin defect +3 more | |
| | | Single nucleotide variant (missense variant) | Budd-Chiari syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | Budd-Chiari syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant) | Budd-Chiari syndrome +3 more | |
| | | Single nucleotide variant (missense variant) | Factor V deficiency +3 more | |
| | | Single nucleotide variant (intron variant) | Factor V deficiency +3 more | |
| | | Single nucleotide variant (missense variant) | Factor V deficiency +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Factor V deficiency +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Factor V deficiency +3 more | |
| | | Single nucleotide variant (intron variant) | Thrombophilia due to activated protein C resistance +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Thrombophilia due to thrombin defect +2 more | |
| | | Single nucleotide variant (missense variant) | Thrombophilia due to activated protein C resistance +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Thrombophilia due to activated protein C resistance +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Factor V deficiency +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Factor V deficiency +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Factor V deficiency +3 more | |
| | | Single nucleotide variant (missense variant) | Budd-Chiari syndrome +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Thrombophilia due to thrombin defect +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Thrombophilia due to activated protein C resistance +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Thrombophilia due to activated protein C resistance +3 more | |
| | | Single nucleotide variant (synonymous variant) | Thrombophilia due to activated protein C resistance +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Budd-Chiari syndrome +3 more | |
| | | Single nucleotide variant (missense variant) | Budd-Chiari syndrome +3 more | |
| | | Single nucleotide variant (missense variant) | Budd-Chiari syndrome +3 more | |
| | | Single nucleotide variant (missense variant) | Thrombophilia due to thrombin defect +2 more | |
| | | Single nucleotide variant (missense variant) | Thrombophilia due to thrombin defect +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Budd-Chiari syndrome +3 more | |
| | | Single nucleotide variant (missense variant) | Thrombophilia due to thrombin defect +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +4 more | |
| | | Single nucleotide variant (missense variant) | Thrombophilia due to thrombin defect +3 more | |
| | | Microsatellite (frameshift variant) | Homocystinuria due to methylene tetrahydrofolate reductase deficiency +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant) | Homocystinuria due to methylene tetrahydrofolate reductase deficiency +4 more | |
| | | Single nucleotide variant (missense variant) | Congenital factor V deficiency +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Congenital factor V deficiency +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Thrombophilia due to thrombin defect +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Factor V deficiency +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Factor V deficiency +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Thrombophilia due to thrombin defect +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Homocystinuria due to methylene tetrahydrofolate reductase deficiency +4 more | |
| | | Single nucleotide variant (missense variant) | Thrombophilia due to thrombin defect +2 more | |
| | | Single nucleotide variant (missense variant) | Neural tube defects, folate-sensitive +3 more | |
| | | Single nucleotide variant (nonsense) | Thrombophilia due to activated protein C resistance +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Deep venous thrombosis +6 more | |
| | | Single nucleotide variant (missense variant) | not provided +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Homocystinuria due to methylene tetrahydrofolate reductase deficiency | |
| | | Single nucleotide variant (synonymous variant) | Neural tube defects, folate-sensitive +6 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Thrombophilia due to thrombin defect +1 more | |
| | | Single nucleotide variant (synonymous variant) | Congenital prothrombin deficiency +1 more | GConflicting classifications of pathogenicity |