RS121909605 FGA

Health Risk Chr 4:154589525
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
FIBRINOGEN ROUEN 1
Familial dysfibrinogenemia
Familial visceral amyloidosis
Ostertag type
Congenital afibrinogenemia
FIBRINOGEN ROUEN 1
Familial dysfibrinogenemia
Familial visceral amyloidosis
Ostertag type
Congenital afibrinogenemia
Other Variants in FGA
rs121909606 rs1403508334 rs121909608 rs121909607 rs78506343 rs587777761 rs121909612 rs121909613 rs121909614 rs587777762
Ask Dr. Hemsworth about this variant