RS6063 FGG
Upload your DNA to see your genotype for this variant.
What This Variant Does
"This is the first snp to experiment with the watson alignment. [OMIM:FIBRINOGEN MILANO XII, DIGENIC...
Associated Conditions
Fibrinogen Milano XII
digenic
Hypofibrinogenemia
Congenital afibrinogenemia
Familial dysfibrinogenemia
Fibrinogen Milano XII
digenic
Hypofibrinogenemia
Congenital afibrinogenemia
Familial dysfibrinogenemia
Other Variants in FGG