RS121909606 FGA

Health Risk Chr 4:154589514
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What This Variant Does
"[OMIM:?]
Associated Conditions
Dysfibrinogenemia
Familial dysfibrinogenemia
FGA-related disorder
Hypofibrinogenemia
Dysfibrinogenemia
Familial dysfibrinogenemia
FGA-related disorder
Hypofibrinogenemia
Other Variants in FGA
rs121909605 rs1403508334 rs121909608 rs121909607 rs78506343 rs587777761 rs121909612 rs121909613 rs121909614 rs587777762
Ask Dr. Hemsworth about this variant