D346G (p.Asp346Gly) variant of FGG (Fibrinogen gamma chain)
D346G (p.Asp346Gly) in FGG (Fibrinogen gamma chain) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as likely pathogenic in the context of Familial dysfibrinogenemia. The record also includes structural context.
D346G (p.Asp346Gly) variant details
- p.Asp346Gly
- rs2530855793
- ClinVar RCV004586097
- Likely pathogenic
- Familial dysfibrinogenemia
- Missense
- ClinVar: Likely pathogenic (Familial dysfibrinogenemia)
- EBI: Likely pathogenic
- UniProt: Likely pathogenic
- Structural context available