RS41267007 PROS1

Health Risk Chr 3:93900833
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Associated Conditions
Thrombophilia due to protein S deficiency
autosomal dominant
autosomal recessive
Protein S deficiency disease
Finnish congenital nephrotic syndrome
PROS1-related disorder
Retinal dystrophy
Thrombophilia due to protein S deficiency
autosomal dominant
autosomal recessive
Protein S deficiency disease
Finnish congenital nephrotic syndrome
PROS1-related disorder
Retinal dystrophy
Other Variants in PROS1
rs121918472 rs121918473 rs121918474 rs267606981 rs2107137679 rs121918475 rs387906674 rs387906675 rs142846443 rs138925964
Ask Dr. Hemsworth about this variant