Congenital heart disease and folate pathway gene polymorphisms: findings from a North Indian cohort.

BMC Cardiovasc Disord · 2026 · PMC12895914 · PMID 41545838

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showed a trendp = 0.07so close (0.05 < p ≤ 0.1)

Family-based association TDT analysis of n = 448 trio CHD families showed a trend for rs1805087 in cyanotic cases ( p = 0.07), particularly driven by TOF ( p = 0.09), with preferential maternal allele transmissions ( p = 0.01, p = 0.05) in the same groups.

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