RS121918479 F2

Health Risk Chr 11:46728138
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What This Variant Does
"[OMIM:?]
Associated Conditions
Congenital prothrombin deficiency
Congenital prothrombin deficiency
Other Variants in F2
rs62623459 rs121918477 rs121918478 rs121918480 rs121918481 rs121918482 rs387906522 rs1799963 rs121918483 rs121918484
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