RS587776837 FGG

Health Risk Chr 4:154612527
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What This Variant Does
"CLNSIG=5
Associated Conditions
Congenital afibrinogenemia
Hypofibrinogenemia
Congenital afibrinogenemia
Hypofibrinogenemia
Other Variants in FGG
rs121913087 rs121913088 rs121913091 rs2066862 rs587776838 rs6063 rs587776839 rs191297318 rs1553965519 rs1553965518
Ask Dr. Hemsworth about this variant