Association of Genetic Variation in the 3'UTR of LHX6, IMMP2L, and AADAC With Tourette Syndrome.

Front Neurol · 2020 · PMC7457023 · PMID 32922348

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hedged sentences

0.0050

closest p · 0.1× alpha

0.0050

boldest claim

The sentences

nominally significantp = 0.005actually significant

For rs7795011 in IMMP2L, we observed a nominally significant over-transmission of T allele in the Greek population ( p = 0.005, χ 2 = 8.0), which withstands 1,000 permutations test ( p = 0.027).

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showed a trendno p-value reported

The top hit of our TDT analysis is rs1042201 of the AADAC gene (nominal p = 0.029), which also showed a trend for association in the meta-analysis.

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