Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121918146
rs121918146
Entrez Id: 5624;105373608
Gene Symbol: PROC;LOC105373608
PROC;LOC105373608
CUI: C0149871
Disease:
Deep Vein Thrombosis
0.010 GeneticVariation BEFREE Protein C deficiency (a novel mutation: ala291Thr) with systemic lupus erythematosus leads to the deep vein thrombosis. 30439769 2018