RS137852283 F9

Health Risk Chr X:139561836
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What This Variant Does
"Changes in this SNP indicate a mutation which occurs at an amino acid evolutionarily conserved in th...
Associated Conditions
Hereditary factor IX deficiency disease
Thrombophilia
X-linked
due to factor 9 defect
Hereditary factor IX deficiency disease
Hereditary factor IX deficiency disease
Thrombophilia
X-linked
due to factor 9 defect
Hereditary factor IX deficiency disease
Other Variants in F9
rs1178811105 rs2148352878 rs2520744315 rs137852223 rs387906474 rs137852226 rs137852227 rs137852228 rs137852229 rs137852230
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