Association between maternal MTHFR and MTRR gene polymorphisms and the risk of congenital heart disease in newborns.

BMC Pediatr · 2026 · PMC13147584 · PMID 41896807

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nominally significantno p-value reported

Analyses of the three SNPs with VSD failed to survive FDR correction in spite of nominally significant findings for rs1801133 in terms of additive and dominant mdoel and for rs1801394 under genotypic model (Supplementary Tables 4–5), while only nominally signficant associations were observed for PDA and rs1801133 specifically under additive and genotypic models (Supplementary Tables 6–7).

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