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Every result shows the extracted entities next to the sentences that support them; rows for the searched entities come first.

Transparent by designEvery result links extracted entities to its source sentence and publication identifier.

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Phenotype

Dyslipidemia

338articles

338mentions

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.

1 records shown · first 60

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
phenotype	dyslipidemia	“The modifiable risk factors include diabetes, hyperlipidemia physical inactivity, and diet, whereas the nonmodifiable include sex, age, and race/ethnicity.”	0.93	phenotype_alias_lexicon_v2
variant	C806T	“In this study, we examined the associations of ANRIL rs1333045 C>T, CYP2C19*17 (C806T, rs12248560C>T, and TCF7L2 rs12255372 G>T with stroke in 100 stroke cases and 100 matched healthy controls from Tabuk population using the amplification refractory mutation system PCR (ARMS-PCR).”	0.82	literature_variant_regex_v2
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