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

Table 5.

SNPs within loci associated with immune system recognized as PD susceptibility factors by GWASs.

Gene/locus SNP MAF (1000 genomes project) Risk allele: OR Study
BST1 Ch 4 rs11724635 g.15737101C>A (intron variant) A = 0.4079 A: OR = 1.126 Nalls et al., 2014
A: OR = 1.15 Nalls et al., 2011
rs4538475 g.15737937A>G c.*195A>G (intron variant) G = 0.3089 OR = 1.24 Satake et al., 2009
rs4698412 g.15737348G>A c.852-328G>A (intron variant) A = 0.4077 OR = 1.14 Pankratz et al., 2012
A: OR = 1.14 Saad et al., 2011
STK39 Ch 2 rs1474055 g.169110394C>T (intergenic variant) T = 0.2007 T: OR = 1.214 Nalls et al., 2014
rs2102808 g.169117025G>T (intergenic variant) T = 0.2083 C: OR = 1.18 Nalls et al., 2011
HLA-DQB1 Ch 6 rs9275326 g.32666660C>T (intergenic variant) T = 0.0843 C: OR = 1.21 Nalls et al., 2014
DDRGK1 Ch 20 rs8118008 g.3168166A>G (downstream gene variant) G = 0.4597 A: OR = 1.111 Nalls et al., 2014

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).

*

Denotes SNPs in 3'-UTR.