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Table 3 Cohorts used for GWAS in this study

From: Genome-wide association studies highlight novel risk loci for septal defects and left-sided congenital heart defects

Cohort

Cases

Controls

FinnGen – General CHD

3506

392,436

UKB – General CHD

2156

484,865

Meta-analysis – General CHD

5662

877,301

FinnGen – conotruncal defects

404

392,942

FinnGen – left-sided lesions

2382

392,503

FinnGen – septal defects

1955

392,428