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. Author manuscript; available in PMC: 2022 Jan 1.
Published in final edited form as: Parkinsonism Relat Disord. 2020 Nov 24;82:109–116. doi: 10.1016/j.parkreldis.2020.11.021

Table 3.

Gene-based burden association tests of candidate genes in 789 ET cases and 770 healthy individuals.

Gene name Sample size N of variants* Total MAC Beta P-value Wald statistic
CCDC183 1559 15 48 −0.2842 0.8599 −1.0798
MMP10 1559 13 37 0.1209 0.3589 0.3615
GPR151 1559 13 19 −0.1075 0.5964 −0.2442
MS4A14 1559 16 43 0.2237 0.2317 0.7332
GEMIN5 1559 31 138 −0.2798 0.9512 −1.6564

Key: ET, Essential tremor; MAC, minor allele count; N, number.

Only exonic deleterious variants (missense, non-sense SNVs) with a minor allele frequency below 1% in gnomAD non-Finnish Europeans exomes were used for the analysis.

Bonferroni corrected p-value threshold for MAF<1% is 0.01.

*

The number of variants in each group is adjusted for specified MAF; in this case, below 0.01.

The total minor allele count (MAC) in a group adjusted for mode of inheritance.