| | | Single nucleotide variant (synonymous variant) | Congenital factor V deficiency +1 more | |
| | | Single nucleotide variant (missense variant) | F5-related condition | |
| | | Single nucleotide variant (missense variant) | not provided +7 more | |
| | | Single nucleotide variant (missense variant) | F5-related condition | |
| | | Single nucleotide variant (synonymous variant) | Inborn genetic diseases +2 more | |
| | | Single nucleotide variant (synonymous variant) | F5-related condition | |
| | | Single nucleotide variant (synonymous variant) | F5-related condition +2 more | |
| | | Single nucleotide variant (synonymous variant) | F5-related condition +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | F5-related condition | |
| | | Single nucleotide variant (synonymous variant) | Thrombophilia due to activated protein C resistance +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Thrombophilia due to thrombin defect +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Budd-Chiari syndrome +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | F5-related condition | |
| | | Single nucleotide variant (missense variant) | F5-related condition +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +8 more | |
| | | Single nucleotide variant (missense variant) | F5-related condition | |
| | | Single nucleotide variant (missense variant) | F5-related condition | |
| | | Single nucleotide variant (missense variant) | Thrombophilia due to thrombin defect +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | F5-related condition | |
| | | Single nucleotide variant (missense variant) | F5-related condition | |
| | | Single nucleotide variant (missense variant) | Thrombophilia due to activated protein C resistance +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | F5-related condition +1 more | |
| | | Single nucleotide variant (missense variant) | F5-related condition | |
| | | Single nucleotide variant (missense variant) | F5-related condition | |
| | | Single nucleotide variant (missense variant) | Thrombophilia due to activated protein C resistance +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | F5-related condition | |
| | | Single nucleotide variant (missense variant) | F5-related condition | |
| | | Single nucleotide variant (missense variant) | Thrombophilia due to activated protein C resistance +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | F5-related condition | |
| | | Single nucleotide variant (synonymous variant) | Factor V deficiency +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | F5-related condition | |
| | | Single nucleotide variant (missense variant) | F5-related condition +2 more | |
| | | Single nucleotide variant (synonymous variant) | Inborn genetic diseases +3 more | |
| | | Single nucleotide variant (missense variant) | F5-related condition | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +2 more | |