rs186899359
This variant is located in the PROCR gene.
▶ClinVar annotation
About PROCR
The protein encoded by this gene is a receptor for activated protein C, a serine protease activated by and involved in the blood coagulation pathway. The encoded protein is an N-glycosylated type I membrane protein that enhances the activation of protein C. Mutations in this gene have been associated with venous thromboembolism and myocardial infarction, as well as with late fetal loss during pregnancy. The encoded protein may also play a role in malarial infection and has been associated with cancer. [provided by RefSeq, Jul 2013]
View all PROCR variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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