RS398122990 F9

Health Risk Chr X:139541073
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What This Variant Does
"rs398122990 is a SNP in the coagulation factor IX F9 gene, in an intron just upstream of the fourth ...
Associated Conditions
Hereditary factor IX deficiency disease
Thrombophilia
X-linked
due to factor 9 defect
Hereditary factor IX deficiency disease
Thrombophilia
X-linked
due to factor 9 defect
Other Variants in F9
rs1178811105 rs2148352878 rs2520744315 rs137852223 rs387906474 rs137852226 rs137852227 rs137852228 rs137852229 rs137852230
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