Association of endothelial nitric oxide synthase (NOS3) rs2070744 variant with advanced retinopathy of prematurity: a case-control study and meta-analysis.

Sci Rep · 2025 · PMC11696690 · PMID 39747280

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did not reach statistical significanceno p-value reported

NOS3 rs1799983 variant The strongest effects of the NOS3 rs1799983T allele on the risk of ROP requiring treatment were found for rs1799983TT homozygotes (OR = 1.4) and the rs2070744TT + CT/rs1799983TT genotype combination (OR = 1.95), although these effects did not reach statistical significance.

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