Beyond the potential common risk gene LRRK2, a genome-wide association study (GWAS) identified an overlap of seven genes presenting a risk for PD with CD (MROH3P, HLA, CCNY, LRRK2, APT, SYMPK and RSPH6A) and four with UC (GUCY1A3, HLA, BTNL2 and TRIM10, Witoelar et al., 2017). This evidence concerns the gene BTNL2 and Parkinson disease.