RS121965064 F11

Health Risk Chr 4:186280257 snv missense variant
Upload your DNA to see your genotype for this variant.
What This Variant Does
"rs121965064, also known as F283L or Phe283Leu, is a SNP in the coagulation factor XI F11 gene. This ...
Associated Conditions
Hereditary factor XI deficiency disease
Factor XI
Plasma factor XI deficiency
F11-related disorder
Hereditary factor XI deficiency disease
Factor XI
Plasma factor XI deficiency
F11-related disorder
Population Frequencies
gnomAD ALL
99.9%
Other Variants in F11
rs373297713 rs121965063 rs1024865708 rs1173748968 rs121965065 rs121965066 rs28934608 rs28934609 rs121965069 rs121965070
Ask Dr. Hemsworth about this variant