| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC126807210, LOC126807211 +1102 more | Copy number gain | See cases | |
| | LOC126807213, LOC126807214 +1068 more | Copy number gain | See cases | |
| | LOC132089068, LOC132089069 +1051 more | Copy number gain | See cases | |
| | LOC126807202, LOC126807203 +1026 more | Copy number gain | See cases | |
| | LOC129993194, LOC129993195 +903 more | Copy number gain | See cases | |
| | LOC123493228, LOC123493229 +481 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | LOC129993250, LOC129993251 +115 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | not provided | |
| | | Single nucleotide variant | FIBRINOGEN-BETA POLYMORPHISM | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Deletion (5 prime UTR variant) | Congenital afibrinogenemia | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Congenital afibrinogenemia | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Congenital afibrinogenemia +1 more | |
| | | Single nucleotide variant (missense variant) | FGB-related disorder | |
| | | Deletion (intron variant) | not specified +1 more | |
| | | 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 (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Hypofibrinogenemia +2 more | |
| | | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (missense variant) | FIBRINOGEN ISE | |
| | | Single nucleotide variant (nonsense) | Hypofibrinogenemia | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Congenital afibrinogenemia | |
| | | Deletion (frameshift variant +1 more) | FGB-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | Congenital afibrinogenemia | |
| | | Single nucleotide variant (synonymous variant +1 more) | Congenital afibrinogenemia | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | FIBRINOGEN NIJMEGEN | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Congenital afibrinogenemia | |
| | | Single nucleotide variant (missense variant +1 more) | Congenital afibrinogenemia | |
| | | Single nucleotide variant (missense variant +1 more) | Familial dysfibrinogenemia | |
| | | Single nucleotide variant (synonymous variant +1 more) | Congenital afibrinogenemia +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | FIBRINOGEN NAPLES | |
| | | Single nucleotide variant (missense variant +1 more) | not specified +2 more | GConflicting classifications of pathogenicity |
| | | Indel (intron variant) | not specified | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Insertion (intron variant) | not provided | |
| | | Indel (intron variant) | not specified | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Single nucleotide variant (synonymous variant +1 more) | Congenital afibrinogenemia +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Congenital afibrinogenemia | |
| | | Single nucleotide variant (synonymous variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | FGB-related disorder +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Familial dysfibrinogenemia | |
| | | Single nucleotide variant (synonymous variant +1 more) | FGB-related disorder | |
| | | Single nucleotide variant (missense variant) | FGB-related disorder | |
| | | Single nucleotide variant (synonymous variant) | FGB-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Abnormal bleeding | |
| | | Single nucleotide variant (splice donor variant) | Familial dysfibrinogenemia | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Deletion (inframe_deletion) | Familial dysfibrinogenemia | |
| | | Single nucleotide variant (missense variant) | Congenital afibrinogenemia | |
| | | Single nucleotide variant (missense variant) | Congenital afibrinogenemia | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Congenital afibrinogenemia | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Hypofibrinogenemia | |
| | | Single nucleotide variant (missense variant) | FGB-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | Congenital afibrinogenemia | |
| | | Single nucleotide variant (missense variant) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | Congenital afibrinogenemia | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Familial dysfibrinogenemia | |
| | | Single nucleotide variant (missense variant) | Familial dysfibrinogenemia +2 more | |
| | | Single nucleotide variant (missense variant) | Congenital afibrinogenemia | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Congenital afibrinogenemia +1 more | |
| | | Single nucleotide variant (missense variant) | Congenital afibrinogenemia +1 more | GConflicting classifications of pathogenicity |