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Phenotype

Infertility

199articles
199mentions
12co-reported genes shown
Most co-reported genes (articles)

Counts are literature co-mentions in SaudiVarKB, not clinical or causal assertions. Gene details: HGNC; variant status: ClinVar via dbSNP.

Publications

1 records shown · first 60

Impact of CYP2A6 genetic polymorphism on letrozole efficacy in Iraqi women with polycystic ovary syndrome.

PMID 40687181 | PMCID PMC12272899 | DOI 10.1016/j.jtumed.2025.06.009 · Journal of Taibah University Medical Sciences · 2025 · 5 validated mentions
TypeEntitySource evidenceConfidenceExtractor
phenotypeinfertility“OBJECTIVES: This study investigated the effects of a genetic polymorphism in CYP2A6 (CYP2A6∗2, 1799T>A) on the therapeutic response to letrozole in Iraqi women with polycystic ovarian syndrome (PCOS)-induced infertility.”0.98phenotype_alias_lexicon_v2
variant1799T>A“OBJECTIVES: This study investigated the effects of a genetic polymorphism in CYP2A6 (CYP2A6∗2, 1799T>A) on the therapeutic response to letrozole in Iraqi women with polycystic ovarian syndrome (PCOS)-induced infertility.”0.82literature_variant_regex_v2
geneCYP2A6“Impact of CYP2A6 genetic polymorphism on letrozole efficacy in Iraqi women with polycystic ovary syndrome.”0.98hgnc_dict_v1
variantrs1801272“Genotyping of CYP2A6∗2 (1799T>A, rs1801272) was performed using allele-specific PCR on blood-derived DNA, and the distribution of wild-type (AA), heterozygous (AT), and mutant (TT) alleles was recorded.”0.90hgvs_regex_v1