Polymorphic Variants of <i>FOXP3</i> Gene (rs 3761548) and (rs 3761549) are Significantly Associated with the Risk for Recurrent Pregnancy Losses. A Study in High Incidence Zone (Kashmir, North India).

J Mother Child · 2025 · PMC12679904 · PMID 41346162

Europe PMC DOI

hedged sentence

—

closest p

—

boldest claim

The sentences

borderline significanceno p-value reported

For FOXP3 gene, rs3761549 C/T, genotypic and allelic distribution portrayed more than 3-fold elevated risk of RPL in women carrying TT genotype than CC genotype ( p = 0.04) but showing borderline significance for T allele between the two groups (cases vs. controls: Table 2 ).

also in 7,017 other papers

Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.

Polymorphic Variants of &lt;i&gt;FOXP3&lt;/i&gt; Gene (rs 3761548) and (rs 3761549) are Significantly Associated with the Risk for Recurrent Pregnancy Losses. A Study in High Incidence Zone (Kashmir, North India).

The sentences

Polymorphic Variants of <i>FOXP3</i> Gene (rs 3761548) and (rs 3761549) are Significantly Associated with the Risk for Recurrent Pregnancy Losses. A Study in High Incidence Zone (Kashmir, North India).