RS762964798 FGA

Health Risk Chr 4:154589500
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Associated Conditions
Hypofibrinogenemia
Familial dysfibrinogenemia
FGA-related disorder
Congenital afibrinogenemia
Familial visceral amyloidosis
Ostertag type
Hypofibrinogenemia
Familial dysfibrinogenemia
FGA-related disorder
Congenital afibrinogenemia
Familial visceral amyloidosis
Ostertag type
Other Variants in FGA
rs121909605 rs121909606 rs1403508334 rs121909608 rs121909607 rs78506343 rs587777761 rs121909612 rs121909613 rs121909614
Ask Dr. Hemsworth about this variant