| | 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 | |
| | | Deletion | Congenital afibrinogenemia | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided | |
| | | Duplication (3 prime UTR variant) | not specified +1 more | |
| | | Deletion (frameshift variant) | Familial visceral amyloidosis, Ostertag type | |
| | | Single nucleotide variant (synonymous variant) | not specified +1 more | |
| | | Single nucleotide variant (missense variant) | FGA-related condition | |
| | | Single nucleotide variant (missense variant) | Congenital afibrinogenemia | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Congenital afibrinogenemia | |
| | | Single nucleotide variant (nonsense) | Familial visceral amyloidosis, Ostertag type +2 more | |
| | | 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 (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | FGA-related condition | |
| | | Single nucleotide variant (missense variant) | FGA-related condition | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Deletion (frameshift variant) | Congenital afibrinogenemia | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Congenital afibrinogenemia | |
| | | Single nucleotide variant (nonsense) | not specified | |
| | | Single nucleotide variant (missense variant) | FGA-related condition +1 more | |
| | | Single nucleotide variant (missense variant) | FGA-related condition | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Congenital afibrinogenemia | |
| | | Single nucleotide variant (missense variant) | Congenital afibrinogenemia | |
| | | Single nucleotide variant (missense variant) | Congenital afibrinogenemia | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | FGA-related condition | |
| | | Duplication (frameshift variant) | See cases | |
| | | Single nucleotide variant (missense variant) | FGA-related condition | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Congenital afibrinogenemia +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Congenital afibrinogenemia +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Congenital afibrinogenemia | |
| | | Single nucleotide variant (missense variant +1 more) | Congenital afibrinogenemia +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Congenital afibrinogenemia | |
| | | Single nucleotide variant (missense variant +1 more) | Familial visceral amyloidosis, Ostertag type +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | FGA-related condition | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Familial visceral amyloidosis, Ostertag type +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not specified | |
| | | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Familial visceral amyloidosis, Ostertag type +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Familial visceral amyloidosis, Ostertag type | |
| | | Deletion (frameshift variant) | Familial dysfibrinogenemia | |
| | | Single nucleotide variant (missense variant) | Familial visceral amyloidosis, Ostertag type +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Congenital afibrinogenemia +3 more | |
| | | Duplication (frameshift variant) | Familial visceral amyloidosis, Ostertag type | |
| | | Deletion (frameshift variant) | not provided | |
| | | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Familial dysfibrinogenemia +3 more | |
| | | Deletion (frameshift variant) | Familial visceral amyloidosis, Ostertag type | |
| | | Deletion (frameshift variant) | Familial visceral amyloidosis, Ostertag type | |
| | | Single nucleotide variant (missense variant) | Familial visceral amyloidosis, Ostertag type | |
| | | Single nucleotide variant (missense variant) | Familial visceral amyloidosis, Ostertag type | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Deletion (frameshift variant) | FGA-related condition | |
| | | Single nucleotide variant (missense variant) | Afibrinogenemia | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Hypofibrinogenemia | |
| | | Single nucleotide variant (missense variant) | Congenital afibrinogenemia | |
| | | Single nucleotide variant (missense variant) | Congenital afibrinogenemia | |
| | | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Congenital afibrinogenemia +2 more | |
| | | Single nucleotide variant (nonsense) | FIBRINOGEN MARBURG | |
| | | Single nucleotide variant (missense variant) | Familial visceral amyloidosis, Ostertag type +2 more | GConflicting classifications of pathogenicity |
| | | Duplication (frameshift variant) | FIBRINOGEN NIEUWEGEIN | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | Familial visceral amyloidosis, Ostertag type +4 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | FGA-related condition | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Familial visceral amyloidosis, Ostertag type +1 more | |