RS199469504 SERPINC1

Health Risk Chr 1:173911933
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What This Variant Does
"CLNSIG=1
Associated Conditions
Hereditary antithrombin deficiency
Hereditary antithrombin deficiency
Other Variants in SERPINC1
rs121909546 rs121909547 rs121909548 rs121909549 rs121909550 rs121909551 rs2227624 rs121909552 rs121909554 rs121909555
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