RS62623459 F2

Health Risk Chr 11:46725897
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
PROTHROMBIN TYPE 3
Congenital prothrombin deficiency
Cerebral palsy
Thrombophilia due to thrombin defect
Pregnancy loss
recurrent
susceptibility to
2
Ischemic stroke
PROTHROMBIN TYPE 3
Congenital prothrombin deficiency
Cerebral palsy
Thrombophilia due to thrombin defect
Pregnancy loss
recurrent
Other Variants in F2
rs121918477 rs121918478 rs121918479 rs121918480 rs121918481 rs121918482 rs387906522 rs1799963 rs121918483 rs121918484
Ask Dr. Hemsworth about this variant