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. 2017 Feb 10;9:20. doi: 10.3389/fnagi.2017.00020

Table 4.

SNPs within loci associated with lysosomal autophagy recognized as PD susceptibility factors by GWASs.

Gene/locus SNP MAF (1000 genomes project) Risk allele: OR Study
GBA/SYT11 Ch 1 rs35749011 g.155135036G>A (intergenic variant) A = 0.0054 A: OR = 1.824 Nalls et al., 2014
i4000416 g.155205634T>C c.1226A>C p.Asn409Ser (missense variant) C = 0.0006 C: OR = 4.05 Do et al., 2011
rs1630500 g.154855055G>A (intergenic variant) A = 0.0559 OR = 1.75 Vacic et al., 2014
rs12726330 g.155108167G>A c.-262G>A (splice region variant) A = 0.0052 OR = 1.71 Pankratz et al., 2012
rs34372695 g.156030037C>T c.-1155C>T (upstream gene variant) T = 0.0088 T: OR = 1.47 Nalls et al., 2011
SCARB2/FAM47E Ch 4 rs6812193 g.77198986C>T c.871-236C>T (intron variant) T = 0.3133 C: OR = 1.1 Nalls et al., 2014
C: OR = 1.19 Do et al., 2011
C: OR = 1.12 Simon-Sanchez et al., 2009

Ch, Chromosome. Data compiled from the GWAS catalog database, the dbSNP and the e!Ensembl (Sherry et al., 2001; Welter et al., 2014; Yates et al., 2016).