RS267606981 PROS1

Health Risk Chr 3:93874245
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What This Variant Does
"aka c.2031A&gt
Associated Conditions
Thrombophilia due to protein S deficiency
autosomal dominant
Thrombophilia due to protein S deficiency
autosomal dominant
Other Variants in PROS1
rs121918472 rs121918473 rs121918474 rs2107137679 rs121918475 rs387906674 rs387906675 rs142846443 rs138925964 rs199469491
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