Associated Variants with R2≤0.3 in the CLHNS Study.
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*: Coordinates are in genome build 37.Bold with †: The most significant p-value among the four methods.Bold without †: The second most significant p-values among the four methods.#: Truth was established by regressing phenotype on true genotypes.Associated Variants with R2≤0.3 in the CLHNS Study.
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2015-12-02
