RS143648758 F11

Health Risk Chr 4:186274198
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What This Variant Does
"CLNSIG=4
Associated Conditions
Hereditary factor XI deficiency disease
Abnormal bleeding
Hereditary factor XI deficiency disease
Abnormal bleeding
Other Variants in F11
rs373297713 rs121965063 rs121965064 rs1024865708 rs1173748968 rs121965065 rs121965066 rs28934608 rs28934609 rs121965069
Ask Dr. Hemsworth about this variant