| | LOC129388668, LOC129388669 +477 more | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Single nucleotide variant (3 prime UTR variant) | Factor XIII, b subunit, deficiency of | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Factor XIII, b subunit, deficiency of | |
| | | Single nucleotide variant (missense variant) | Factor XIII, b subunit, deficiency of | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Factor XIII, b subunit, deficiency of | |
| | | Single nucleotide variant (missense variant) | not specified +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Factor XIII, b subunit, deficiency of +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Factor XIII, b subunit, deficiency of | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Indel (frameshift variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Microsatellite (intron variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Factor XIII, b subunit, deficiency of +1 more | |
| | | Single nucleotide variant (missense variant) | Thrombus | |
| | | Single nucleotide variant (missense variant) | Factor XIII, b subunit, deficiency of | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (intron variant) | Factor XIII, b subunit, deficiency of +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Microsatellite (inframe_indel +1 more) | Factor XIII, b subunit, deficiency of | |
| | | Single nucleotide variant (missense variant) | Cholesteatoma | |
| | | Deletion (frameshift variant) | Factor XIII, b subunit, deficiency of | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Deletion (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Factor XIII, b subunit, deficiency of | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | Factor XIII, b subunit, deficiency of +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Factor XIII, b subunit, deficiency of | |
| | | Single nucleotide variant (missense variant) | Factor XIII, b subunit, deficiency of | |
| | | Single nucleotide variant (synonymous variant) | Factor XIII, b subunit, deficiency of | |
| | | Single nucleotide variant (missense variant) | Factor XIII, b subunit, deficiency of | |
| | | Single nucleotide variant (synonymous variant) | F13B-related condition | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Hereditary factor XIII deficiency disease +2 more | |
| | | Duplication (frameshift variant) | Factor XIII, b subunit, deficiency of | |
| | | Single nucleotide variant (missense variant) | Factor XIII, b subunit, deficiency of | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Factor XIII, b subunit, deficiency of | |
| | | Single nucleotide variant (synonymous variant) | Factor XIII, b subunit, deficiency of | |
| | | Single nucleotide variant (synonymous variant) | Factor XIII, b subunit, deficiency of +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Factor XIII, b subunit, deficiency of | |
| | | Single nucleotide variant (missense variant) | Factor XIII, b subunit, deficiency of | |
| | | Duplication (nonsense +1 more) | F13B-related condition | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Factor XIII, b subunit, deficiency of +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Factor XIII, b subunit, deficiency of | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Factor XIII, b subunit, deficiency of | |
| | | Single nucleotide variant (missense variant) | Factor XIII, b subunit, deficiency of | |
| | | Single nucleotide variant (missense variant) | Factor XIII, b subunit, deficiency of | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Factor XIII, b subunit, deficiency of | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (splice donor variant) | Factor XIII, b subunit, deficiency of | |
| | | Single nucleotide variant (missense variant) | Factor XIII, b subunit, deficiency of | |
| | | Single nucleotide variant (missense variant) | Factor XIII, b subunit, deficiency of | |
| | | Single nucleotide variant (synonymous variant) | Factor XIII, b subunit, deficiency of +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Factor XIII, b subunit, deficiency of | |
| | | Deletion (inframe_deletion) | Factor XIII, b subunit, deficiency of | |
| | | Single nucleotide variant (missense variant) | Factor XIII, b subunit, deficiency of | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | Factor XIII, b subunit, deficiency of | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | Factor XIII, b subunit, deficiency of | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | Factor XIII, b subunit, deficiency of +2 more | |
| | | Deletion (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not specified | |