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Molecular Role of Asn680Ser and Asp37Glu Missense Variants in Saudi Women with Female Infertility and Polycystic Ovarian Syndrome.

PMID 37504264 | PMCID PMC10378235 | DOI 10.3390/cimb45070348 · Current issues in molecular biology · 2023 · 5 validated mentions
TypeEntitySource evidenceConfidenceExtractor
variantrs6166“Based on the documented missense variants, rs6166 and rs2296545 single-nucleotide polymorphisms (SNPs) were not identified in Saudi women with FI and PCOS.”0.90hgvs_regex_v1
geneRNLS“The renalase gene (RNLS) is associated with FI and other human diseases.”0.98hgnc_dict_v1
phenotypeinfertility“Molecular Role of Asn680Ser and Asp37Glu Missense Variants in Saudi Women with Female Infertility and Polycystic Ovarian Syndrome.”0.98phenotype_alias_lexicon_v2
populationSaudi Arabia“Molecular Role of Asn680Ser and Asp37Glu Missense Variants in Saudi Women with Female Infertility and Polycystic Ovarian Syndrome. Based on the documented missense variants, rs6166 and rs2296545 single-nucleotide polymorphisms (SNPs) were not identified in Saudi women with FI and PCOS. This study aimed to investigate the molecular role of the two SNPs in Saudi women with FI and PCOS. In this cross-sectional study, 96 healthy controls, 96 women with FI, and 96 women with PCOS were recruited. Both rs6166 and rs2296545 had no role in FI or PCOS in Saudi women. A predicted reason for non-association in Saudi women could be the role of elderly women in the controls compared with women with FI and PCOS. In conclusion, rs6166 and rs2296545 SNPs were not associated with FI or PCOS in Saudi women.”0.95saudi_context_rules_v1