Summary data for top variants with suggestive inherited or maternal association with conotruncal heart defects.

AChromosome.BHg18/NCBI build 36.CMinor allele frequency among non-Hispanic white study participant founders (i.e. mother and father).DFor SNPs mapping within genes, gene names are listed, and for intergenic SNPs, the nearest gene is listed in parentheses.ERelative risk estimate for carrying one copy of the high-risk allele compared to no copies, and corresponding 95% confidence interval.FImputed SNP; concordance between the imputed and assay-based genotypes in 21 samples from the discovery sample that were genotyped with the follow-up sample was 98.5%.