RS121909607 FGA

Health Risk Chr 4:154589513
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What This Variant Does
"[OMIM:?]
Associated Conditions
Dysfibrinogenemia
Hypofibrinogenemia
Abnormal bleeding
Familial dysfibrinogenemia
Familial visceral amyloidosis
Ostertag type
Congenital afibrinogenemia
FGA-related disorder
Hypofibrinogenemia
Dysfibrinogenemia
Hypofibrinogenemia
Abnormal bleeding
Familial dysfibrinogenemia
Familial visceral amyloidosis
Ostertag type
Other Variants in FGA
rs121909605 rs121909606 rs1403508334 rs121909608 rs78506343 rs587777761 rs121909612 rs121909613 rs121909614 rs587777762
Ask Dr. Hemsworth about this variant