| | LOC123493236, LOC123493237 +1310 more | Copy number gain | See cases | |
| | LOC132089056, LOC132089057 +1245 more | Copy number gain | See cases | |
| | LOC126807228, LOC126807229 +1102 more | Copy number gain | See cases | |
| | LOC129993256, LOC129993257 +1068 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | 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 condition | |
| | | 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) | not provided +2 more | |
| | | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (missense variant) | FIBRINOGEN ISE | |
| | | Single nucleotide variant (nonsense) | Hypofibrinogenemia | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | Congenital afibrinogenemia | |
| | | Deletion (frameshift variant +1 more) | FGB-related condition | |
| | | 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 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 (missense variant +1 more) | FGB-related condition +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Familial dysfibrinogenemia | |
| | | Single nucleotide variant (synonymous variant +1 more) | FGB-related condition | |
| | | Single nucleotide variant (missense variant) | FGB-related condition | |
| | | Single nucleotide variant (synonymous variant) | FGB-related condition +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 condition +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) | Familial dysfibrinogenemia +2 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant) | FGB-related condition +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant) | Thrombus +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Familial dysfibrinogenemia | |
| | | Single nucleotide variant (intron variant) | not provided | |