RS200378626 FGA

Health Risk Chr 4:154586012
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Associated Conditions
Congenital afibrinogenemia
Familial visceral amyloidosis
Ostertag type
Inborn genetic diseases
Familial dysfibrinogenemia
Congenital afibrinogenemia
Familial visceral amyloidosis
Ostertag type
Inborn genetic diseases
Familial dysfibrinogenemia
Other Variants in FGA
rs121909605 rs121909606 rs1403508334 rs121909608 rs121909607 rs78506343 rs587777761 rs121909612 rs121909613 rs121909614
Ask Dr. Hemsworth about this variant