RS886039906 F8

Health Risk Chr X:154929022
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What This Variant Does
"CLNSIG=4
Associated Conditions
Hereditary factor VIII deficiency disease
Hereditary factor VIII deficiency disease
Other Variants in F8
rs137852354 rs137852355 rs137852356 rs137852357 rs137852358 rs137852359 rs137852360 rs28937294 rs28935499 rs137852361
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