RS149599496 FGB

Health Risk Chr 4:154567784
Upload your DNA to see your genotype for this variant.
Associated Conditions
Familial dysfibrinogenemia
Congenital afibrinogenemia
Inborn genetic diseases
Familial dysfibrinogenemia
Congenital afibrinogenemia
Inborn genetic diseases
Other Variants in FGB
rs770246669 rs1578785111 rs1578783532 rs187641148 rs111502670 rs1282469317 rs1730132238 rs2530766247 rs2530775972 rs2227434
Ask Dr. Hemsworth about this variant