RS28935203 F8

Health Risk Chr X:154928694
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What This Variant Does
"[OMIM:[[Hemophilia]] A]
Associated Conditions
Hereditary factor VIII deficiency disease
Inborn genetic diseases
Hereditary factor VIII deficiency disease
Hereditary factor VIII deficiency disease
Inborn genetic diseases
Hereditary factor VIII deficiency disease
Other Variants in F8
rs137852354 rs137852355 rs137852356 rs137852357 rs137852358 rs137852359 rs137852360 rs28937294 rs28935499 rs137852361
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