Imputation of Variants from the 1000 Genomes Project Modestly Improves Known Associations and Can Identify Low-frequency Variant - Phenotype Associations Undetected by HapMap Based Imputation (original) (raw)
Table 5
The 13 signals identified as having an associated 1000 Genomes-based imputed SNP reaching genome-wide significance where the best HapMap SNP did not, ordered by minor allele frequency group (<5% or ≥5) and the minor allele frequency of the 1000 Genomes SNP.