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3 records shown · first 60

PMID 41908226 | PMCID PMC13018941 | DOI 10.1016/j.jtumed.2026.03.003 · Journal of Taibah University Medical Sciences · 2026 · 10 validated mentions

Evidence preview

Type	Entity	Source evidence	Confidence	Extractor
variant	rs12248560	“Five detected variants had high frequencies: rs7067866, rs7916649, rs4917623, rs12248560, and rs11188072.”	0.90	hgvs_regex_v1
gene	CYP2C19	“Genetic variants of CYP2C19 and CYP2C18 and their clinical implications in the Saudi population.”	0.98	hgnc_dict_v1
gene	CYP2C18	“Genetic variants of CYP2C19 and CYP2C18 and their clinical implications in the Saudi population.”	0.98	hgnc_dict_v1
population	Saudi Arabia	“Genetic variants of CYP2C19 and CYP2C18 and their clinical implications in the Saudi population. BACKGROUND: At least 500 genetic polymorphisms associated with the CYP2C19 and CYP2C18 enzymes have been identified, yet few polymorphisms have been measured in the Saudi population. Blood samples from 374 Saudi adults were genotyped. Tens of previously unmeasured CYP2C19 and CYP2C18 variants were identified in the Saudi population.”	0.95	saudi_context_rules_v1

PMID 41247572 | PMCID PMC12623554 | DOI 10.1007/s10571-025-01625-2 · Cellular and molecular neurobiology · 2025 · 11 validated mentions

Evidence preview

Type	Entity	Source evidence	Confidence	Extractor
variant	rs12248560	“In addition, the CT genotype and T allele of the CYP2C19*17 (rs12248560) C>T were also associated stroke with OR = 2, P value = 0.02 and OR = 2.3, P value = 0.002, respectively.”	0.90	hgvs_regex_v1
gene	CYP2C19	“Comprehensive Molecular Evaluation of Transcription Factor 7-like 2, Long Noncoding RNA (ANRIL), and CYP2C19*17 Gene Variants and Their Association with Predisposition and Progression in Stroke Patients.”	0.98	hgnc_dict_v1
gene	TCF7L2	“The Transcription factor 7-like 2 (TCF7L2) has crucial roles in biological and pathological processes such as inflammation, metabolism, and atherosclerosis.”	0.98	hgnc_dict_v1
phenotype	stroke	“Comprehensive Molecular Evaluation of Transcription Factor 7-like 2, Long Noncoding RNA (ANRIL), and CYP2C19*17 Gene Variants and Their Association with Predisposition and Progression in Stroke Patients.”	0.98	phenotype_alias_lexicon_v2

PMID 38004282 | PMCID PMC10672292 | DOI 10.3390/life13112142 · Life (Basel, Switzerland) · 2023 · 10 validated mentions

Evidence preview

Type	Entity	Source evidence	Confidence	Extractor
variant	rs12248560	“In this study, we examined the link between single nucleotide variations (SNVs) of TNF-α-rs1800629 G>A, CYP2C19*17 (rs12248560) C>T, and miR-423 rs6505162 C>A and the expression of TNF-α with CAD.”	0.90	hgvs_regex_v1
gene	CYP2C19	“Differential Expression of Serum Proinflammatory Cytokine TNF-α and Genetic Determinants of TNF-α, CYP2C19*17, miR-423 Genes and Their Effect on Coronary Artery Disease Predisposition and Progression.”	0.98	hgnc_dict_v1
phenotype	coronary artery disease	“Differential Expression of Serum Proinflammatory Cytokine TNF-α and Genetic Determinants of TNF-α, CYP2C19*17, miR-423 Genes and Their Effect on Coronary Artery Disease Predisposition and Progression.”	0.98	phenotype_alias_lexicon_v2
phenotype	obesity	“Risk factors for CAD include older age, male gender, obesity, high blood pressure, smoking, diabetes, hyperlipidemia, and genetic factors.”	0.98	phenotype_alias_lexicon_v2