| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | F10-related disorder | |
| | | Single nucleotide variant (missense variant) | Hereditary factor X deficiency disease | |
| | | Single nucleotide variant (missense variant) | Hereditary factor X deficiency disease | |
| | | Single nucleotide variant (missense variant) | Hereditary factor X deficiency disease | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Hereditary factor X deficiency disease | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Deletion (frameshift 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 | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Insertion (intron variant) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | Factor X deficiency | |
| | | Single nucleotide variant (missense variant) | Factor X deficiency | |
| | | Deletion (frameshift variant) | Factor X deficiency | |
| | | Single nucleotide variant (missense variant) | Factor X deficiency | |
| | | Single nucleotide variant (missense variant) | Factor X deficiency | |
| | | Single nucleotide variant (missense variant) | Factor X deficiency | |
| | | Single nucleotide variant (missense variant) | Factor X deficiency | |
| | | Single nucleotide variant (missense variant) | Factor X deficiency | |
| | | Single nucleotide variant (missense variant) | Factor X deficiency | |
| | | Single nucleotide variant (missense variant +1 more) | Factor X deficiency | |
| | | Single nucleotide variant (missense variant +1 more) | Abnormal bleeding +1 more | |
| | | Single nucleotide variant (missense variant) | Hereditary factor X deficiency disease +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Hereditary factor X deficiency disease +1 more | |
| | | Single nucleotide variant (intron variant) | Hereditary factor X deficiency disease +1 more | |
| | | Single nucleotide variant (missense variant) | Hereditary factor X deficiency disease | |
| | | Single nucleotide variant (missense variant) | Factor X deficiency +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant | Factor x deficiency, autosomal dominant | |
| | | Single nucleotide variant (missense variant) | Factor X deficiency | |
| | | Single nucleotide variant (missense variant) | Factor X deficiency | |
| | | Single nucleotide variant | Factor X deficiency | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | Factor X deficiency | |