RS121964946 F10

Health Risk Chr 13:113147496
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What This Variant Does
"[OMIM:?]
Associated Conditions
Factor x deficiency
autosomal dominant
Factor x deficiency
autosomal dominant
Other Variants in F10
rs104894392 rs387906506 rs121964947 rs121964940 rs753790195 rs121964948 rs121964941 rs61753266 rs121964942 rs121964943
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