Genetic Variants in Preeclampsia During Pregnancy: A Hospital-Based Case–Control Study

<b><b>Background/Objectives:</b></b> Preeclampsia is a multifactorial disorder with a possible genetic component. While numerous studies have explored genetic susceptibility, validation remains inconsistent. The aim was to assess the association between hypertension-related polymorphisms and preeclampsia risk. <b>Methods</b>: A case-control study was conducted in Karaganda, Kazakhstan (n = 95). Sixty SNPs were genotyped using the QuantStudio™ 12K Flex system. Genotype-phenotype associations were evaluated using five inheritance models and statistical analysis in R. <b>Results</b>: Significant associations were found for rs2516839 (C/T: OR = 5.28; 95% CI: 1.53-18.15), rs17672135 (T/T: OR = 3.48; CI: 1.05-11.5), and rs10757278 (A/G: OR = 0.3; CI: 0.11-0.83). However, wide confidence intervals suggest potential limitations in sample size and generalizability. <b>Conclusions</b>: While these polymorphisms show promise as genetic markers of preeclampsia risk, their clinical application requires further validation in larger, multi-ethnic cohorts.