RS121918158 PROC

Health Risk Chr 2:127428575
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What This Variant Does
"aka c.1015G&gt
Associated Conditions
Thrombophilia due to protein C deficiency
autosomal dominant
Inborn genetic diseases
Thrombophilia due to protein C deficiency
autosomal dominant
Inborn genetic diseases
Other Variants in PROC
rs121918141 rs121918142 rs121918143 rs121918144 rs121918145 rs121918146 rs121918147 rs121918148 rs121918149 rs121918150
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