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. 2020 Jul 11;24(15):8744–8752. doi: 10.1111/jcmm.15508

TABLE 2.

Association of SNPs of candidate genes and odds ratio to PD risk

Candidate gene SNP Effect allele Allele model a Dominant model b Recessive model b Additive model b
P OR (95% CI) P OR (95% CI) P OR (95% CI) P OR (95% CI)
SNCA rs8180209 A .047 0.77 (0.60, 0.98) .138 0.74 (0.50, 1.10) .077 0.66 (0.42, 1.05) .047 0.77 (0.59, 0.99)
MCCC1 rs2270968 G .091 1.27 (0.99, 1.64) .024 1.52 (1.06‐2.19) .907 0.96 (0.50, 1.84) .084 1.28 (0.97, 1.71)
DLG2 rs7479949 C .159 0.82 (0.64, 1.06) .322 0.82 (0.56, 1.21) .019 0.26 (0.09‐0.80) .072 0.73 (0.52, 1.03)
GBF1 rs10748818 G .043 0.72 (0.56, 0.92) .093 0.73 (0.50, 1.05) .089 0.60 (0.33, 1.08) <.001 c 0.37 (0.25‐0.57)
MBNL2 rs4771268 T .011 0.72 (0.54, 0.96) .179 0.77 (0.53, 1.12) .003 c 0.48 (0.29‐0.78) .015 0.73 (0.56‐0.94)

Abbreviations: CI, confidence interval; OR, odds ratio; PD, Parkinson's disease; SNP, single nucleotide polymorphism.

a

P value, OR and 95% CI were obtained from risk analysis and refer to the risk allele.

b

Adjusted for age and gender.

c

The statistical significances remained after using Bonferroni correction.

Bold values are indicate the significant results