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Exploring the association of ESR1 and ESR2 gene SNPs with polycystic ovary syndrome in human females: a comprehensive association study.

PMID 38281964 | PMCID PMC10823698 | DOI 10.1186/s13048-023-01335-7 · Journal of ovarian research · 2024 · 18 validated mentions
TypeEntitySource evidenceConfidenceExtractor
variantrs1467954450“Variants rs1467954450 (ESR1) and rs140630557 (ESR2) were identified to reduce the binding tendency of ESRα and β receptors with estradiol as reflected by the docking scores i.e. -164.97 and -173.23, respectively.”0.90hgvs_regex_v1
geneESR1“Exploring the association of ESR1 and ESR2 gene SNPs with polycystic ovary syndrome in human females: a comprehensive association study.”0.98hgnc_dict_v1
geneESR2“Exploring the association of ESR1 and ESR2 gene SNPs with polycystic ovary syndrome in human females: a comprehensive association study.”0.98hgnc_dict_v1
phenotypeinfertility“BACKGROUND: Polycystic Ovary Syndrome (PCOS) affects a significant proportion of human females worldwide and is characterized by hormonal, metabolic, and reproductive dysfunctions, including infertility, irregular menstrual cycles, acanthosis nigricans, and hirsutism.”0.98phenotype_alias_lexicon_v2