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Association analyses were performed in an additive model (SNP1, SNP2 and SNP3) and a recessive model (SNP1, SNP2, SNP3 and haplotype). SNP1 (912G>A) was associated with PD (P=0.004, OR=1.31, 95% CI 1.08-1.59) and its risk association was stronger in patients younger than 65years (P=0.004, OR=1.54, 95% CI 1.12-2.11). SNP3 (1438T>G) was not associated with PD (P=0.135, OR=1.22, 95% CI 0.93-1.59). SNP2 (Ile➔Val) was not associated with PD (P=0.369, OR=1.12, 95% CI 0.90-1.40), but was significantly over-represented in PD patients (P=0.018). The recessive model showed that the wild-type haplotype CCT (SNP1, SNP2, SNP3) was significantly over-represented in PD patients (P=0.0025, OR=2.31, 95% CI 1.35-3.94), but not in controls (P=0.58, OR=0.89, 95% CI 0.71-1.13). All four SNPs were in Hardy-Weinberg equilibrium. We confirmed an association of BDNF SNP1 with PD in a German cohort. 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