RS5017717 PROS1

Health Risk Chr 3:93884869
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What This Variant Does
"CLNSIG=1
Associated Conditions
Thrombophilia due to protein S deficiency
autosomal recessive
Protein S deficiency disease
autosomal dominant
Thrombophilia due to protein S deficiency
autosomal recessive
Protein S deficiency disease
autosomal dominant
Other Variants in PROS1
rs121918472 rs121918473 rs121918474 rs267606981 rs2107137679 rs121918475 rs387906674 rs387906675 rs142846443 rs138925964
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