RS146387238 FGA

Health Risk Chr 4:154587511
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Congenital afibrinogenemia
Familial hypodysfibrinogenemia
Hypofibrinogenemia
Familial dysfibrinogenemia
Familial visceral amyloidosis
Ostertag type
Congenital afibrinogenemia
Familial hypodysfibrinogenemia
Hypofibrinogenemia
Familial dysfibrinogenemia
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