RS387906452 F8

Health Risk Chr X:154929666
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary factor VIII deficiency disease
Thrombophilia
X-linked
due to factor 8 defect
Hereditary factor VIII deficiency disease
Thrombophilia
X-linked
due to factor 8 defect
Other Variants in F8
rs137852354 rs137852355 rs137852356 rs137852357 rs137852358 rs137852359 rs137852360 rs28937294 rs28935499 rs137852361
Ask Dr. Hemsworth about this variant