Genetic Variants in SNCA and the Risk of Sporadic Parkinson’s Disease and Clinical Outcomes: A Review

Figure 1

Diagram illustrating the locations of the main SNPs in human SNCA gene reviewed in the present study: SNCA-REP1 (promoter region), rs2736990 (intron 4), rs356165 (3′ UTR), and rs356219, rs356220, and rs11931074 (3′ end). Black boxes indicate translated exons, grey boxes indicate untranslated regions, and the white line indicates introns.