Barely Significant
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Paraoxonase single nucleotide variants show associations with polycystic ovary syndrome: a meta-analysis.

Reprod Biol Endocrinol · 2020 · PMC7678182 · PMID 33218342

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highly significantno p-value reported
These two core LD1 findings conferred greater odds of PCOS to the var allele in the highly significant ( P a < 0.0001) overall (OR 1.44, 95% CI 1.24–1.67) and Asian (OR 1.41, 95% CI 1.20–1.65) outcomes.

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