RS373297713 F11

Health Risk Chr 4:186287824
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What This Variant Does
"rs373297713, better known as c.1716 1G&gt
Associated Conditions
Hereditary factor XI deficiency disease
Plasma factor XI deficiency
Clear cell carcinoma of kidney
Hereditary factor XI deficiency disease
Plasma factor XI deficiency
Clear cell carcinoma of kidney
Other Variants in F11
rs121965063 rs121965064 rs1024865708 rs1173748968 rs121965065 rs121965066 rs28934608 rs28934609 rs121965069 rs121965070
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