RS121913088 FGG

Health Risk Chr 4:154606932
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
FIBRINOGEN HAIFA 1
Hypofibrinogenemia
Familial dysfibrinogenemia
Congenital afibrinogenemia
FIBRINOGEN HAIFA 1
Hypofibrinogenemia
Familial dysfibrinogenemia
Congenital afibrinogenemia
Other Variants in FGG
rs121913087 rs121913091 rs2066862 rs587776837 rs587776838 rs6063 rs587776839 rs191297318 rs1553965519 rs1553965518
Ask Dr. Hemsworth about this variant