RS531225271 F7

Health Risk Chr 13:113118758
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Factor VII deficiency
Congenital factor VII deficiency
F7-related disorder
Myocardial infarction
susceptibility to
Factor VII deficiency
Congenital factor VII deficiency
F7-related disorder
Myocardial infarction
susceptibility to
Other Variants in F7
rs121964928 rs121964930 rs121964932 rs1056071555 rs387906507 rs36209567 rs786205091 rs6046 rs1263426144 rs121964933
Ask Dr. Hemsworth about this variant