RS786204429 F11

Health Risk Chr 4:186280517
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What This Variant Does
"CLNSIG=4
Associated Conditions
Hereditary factor XI deficiency disease
Plasma factor XI deficiency
F11-related disorder
Inborn genetic diseases
Hereditary factor XI deficiency disease
Plasma factor XI deficiency
F11-related disorder
Inborn genetic diseases
Other Variants in F11
rs373297713 rs121965063 rs121965064 rs1024865708 rs1173748968 rs121965065 rs121965066 rs28934608 rs28934609 rs121965069
Ask Dr. Hemsworth about this variant