| | | Single nucleotide variant | Hereditary factor X deficiency disease | |
| | | Single nucleotide variant (5 prime UTR variant) | Hereditary factor X deficiency disease | |
| | | Single nucleotide variant (missense variant) | Hereditary factor X deficiency disease | |
| | | Single nucleotide variant (synonymous variant) | Hereditary factor X deficiency disease +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Hereditary factor X deficiency disease +1 more | |
| | | Single nucleotide variant (missense variant) | Hereditary factor X deficiency disease +1 more | |
| | | Single nucleotide variant (synonymous variant) | Hereditary factor X deficiency disease +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Factor X deficiency +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Hereditary factor X deficiency disease | |
| | | Single nucleotide variant (synonymous variant) | Hereditary factor X deficiency disease | |
| | | Single nucleotide variant (synonymous variant) | Hereditary factor X deficiency disease | |
| | | Single nucleotide variant (synonymous variant) | Hereditary factor X deficiency disease | |
| | | Single nucleotide variant (synonymous variant +1 more) | F10-related condition +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Factor X deficiency +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary factor X deficiency disease | |
| | | Single nucleotide variant (missense variant) | Hereditary factor X deficiency disease +1 more | |
| | | Single nucleotide variant (missense variant) | Hereditary factor X deficiency disease | |
| | | Single nucleotide variant (synonymous variant) | F10-related condition +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hereditary factor X deficiency disease | |
| | | Single nucleotide variant (intron variant) | Hereditary factor X deficiency disease | |
| | | Single nucleotide variant (synonymous variant) | Hereditary factor X deficiency disease +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Hereditary factor X deficiency disease | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary factor X deficiency disease | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense +1 more) | Hereditary factor X deficiency disease | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary factor X deficiency disease +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary factor X deficiency disease | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary factor X deficiency disease | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary factor X deficiency disease | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary factor X deficiency disease | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |