README for GCST0044540 significant loci

This document describes the column headers for GCST0044540 significant loci data

chromosome = The chromosome that the variant is located on
variant_id = The rsid of the variant
base_pair_location = The base pair location of the variant
effect_allele = The effect allele of the variant
other_allele = The non-effect allele
N = per allele sample size
effect_allele_frequency = Frequency of the effect allele in the control population
T = GLMM score statistic
SE_T = standard error of the score statistic
P_noSPA = raw p-value
beta = SNP effect or log(odds ratio)
standard_error = standard error for the estimated effect size after the SPA correction
p_value = p-value after the SPA correction
CONVERGE = to indicate whether the SPA correction is converged for the variant