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Table 4 The number of scoring SNPs that fall into each p-value threshold based on the discovery set is shown.

From: Recent methods for polygenic analysis of genome-wide data implicate an important effect of common variants on cardiovascular disease risk

Target GWAS Statistics for Each Scoring SNP Set  
P-Value Threshold Range Number of SNPs P-Value Adjusted R2
> 0-.1 24843 0.4974 0
> .1-.2 24201 0.8096 0
> .2-.3 24329 0.00393* 0.004177
> .3-.4 23962 0.971 0
> .4-.5 24269 0.032033* 0.002056
> .5-.6 24500 0.06449 0.001383
> .6-.7 24429 0.7129 0
> .7-.8 24429 0.23410 0.0002382
> .8-.9 24397 0.444 0
> .9-1 24508 0.7921 0
  1. Significant ranges and their respective p-values are highlighted.