RS121909567 SERPINC1

Health Risk Chr 1:173914570
Upload your DNA to see your genotype for this variant.
What This Variant Does
"rs121909567, also known as c.391C&gt
Associated Conditions
Hereditary antithrombin deficiency
Deep venous thrombosis
Hereditary antithrombin deficiency
Deep venous thrombosis
Other Variants in SERPINC1
rs121909546 rs121909547 rs121909548 rs121909549 rs121909550 rs121909551 rs2227624 rs121909552 rs121909554 rs121909555
Ask Dr. Hemsworth about this variant