RS1553965518 FGG

Health Risk Chr 4:154606804
Upload your DNA to see your genotype for this variant.
Associated Conditions
Inborn genetic diseases
Familial dysfibrinogenemia
Inborn genetic diseases
Familial dysfibrinogenemia
Other Variants in FGG
rs121913087 rs121913088 rs121913091 rs2066862 rs587776837 rs587776838 rs6063 rs587776839 rs191297318 rs1553965519
Ask Dr. Hemsworth about this variant