Nationwide French Study of <i>RET</i> Variants Detected from 2003 to 2013 Suggests a Possible Influence of Polymorphisms as Modifiers

Abstract

The findings propose a classification of 15 of the 26 VUS in RET without any well-defined risk profiles and suggest that the G691S SNP, or a combination of SNPs, may be associated with the development of PHEO.