Results of genome-wide case control association analyses using latent class membership as phenotype.

This table gives the SNP phenotype associations that reached or approached the genome-wide level of significance (after correction for multiple testing using the Bonferroni method). The position of the SNPs on the chromosomes is given in base pairs according to the Ensemble database, assembly GRCh37.p2, Feb 2009, Version 60.37e. SNP, single nucleotide polymorphism; LC1, Latent Class 1; LC2, Latent Class 2, Chr., chromosome; Corr P, p-value of the correlation-trend test, Bonf. P, Bonferroni corrected p-value.