Gene entry
FGG
fibrinogen gamma chain
- Chromosome
- 4
- Cytoband
- 4q32.1
- Variants (rsID)
- 13
FGG is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 4 (region 4q32.1). Its official name is “fibrinogen gamma chain”. The reference table lists 13 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs2066865Benignsingle nucleotide variantCongenital afibrinogenemia
- rs6063Conflicting interpretationssingle nucleotide variantFibrinogen Milano XII, digenic|Hypofibrinogenemia|Congenital afibrinogenemia|Familial dysfibrinogenemia
- rs78257946Likely pathogenicsingle nucleotide variantHypofibrinogenemia|Familial dysfibrinogenemia
- rs121913090Othersingle nucleotide variantFIBRINOGEN BALTIMORE 3
- rs121913088Pathogenicsingle nucleotide variantFIBRINOGEN HAIFA 1|Hypofibrinogenemia|Familial dysfibrinogenemia
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.