aMajor/minor allele; bCalculated by additive model; cP for heterogeneity. Stratified analysis on the associations between four SNPs in EPRS with congenital heart disease.
Mutations in Lamin A/C (LMNA) cause a heterogeneous group of genetic disorders named as laminopathies. LMNA, an inner nuclear membrane protein, is implicated in nuclear genome organization and gene ex
Results from logistic regression fits of the following 2 models. Marginal Model for each SNP: History of lone AF using as covariates Sex +4 principal components of genetic sharing. Full Model for each
