We selected four P -value thresholds (all SNPs, P T < 0.5, P T < 0.05, and P T < 0.005) to represent nominal uncorrected significance ( P < 0.05), SNPs within an order of magnitude more or less significant, and a model with all SNPs.
← all excerpts
Pharmacological enrichment of polygenic risk for precision medicine in complex disorders.
1
—
—