Correction: Association of Folate-Pathway Gene Polymorphisms with the Risk of Prostate Cancer: a Population-Based Nested Case-Control Study, Systematic Review, and Meta-analysis

In this article (1), which was published in the September 2009 issue of Cancer Epidemiology, Biomarkers & Prevention, the FOLH1 SNP rs202676 was referred to incorrectly as FOLH1 “1561T>C.” The correct designation is as follows:

rs202676 occurs in exon 2 of FOLH1/GCPII (referred to as 223T>C or 484T>C), corresponding to amino acid substitution Y75H. The 1561C>T polymorphism (also referred to as 1684C>T) occurs in exon 13 of FOLH1, is identified as rs61886492, and corresponds to amino acid substitution H475Y.