RS542967227 F11

Health Risk Chr 4:186285765
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary factor XI deficiency disease
Plasma factor XI deficiency
Hereditary factor XI deficiency disease
Plasma factor XI deficiency
Other Variants in F11
rs373297713 rs121965063 rs121965064 rs1024865708 rs1173748968 rs121965065 rs121965066 rs28934608 rs28934609 rs121965069
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