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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.
Publications
1 records shown · first 60Vitamin D Related Gene Polymorphisms and Cholesterol Levels in a Mediterranean Population.
PMID 35448078 | PMCID PMC9028837 | DOI 10.3390/jcdd9040102 · Journal of cardiovascular development and disease · 2022 · 3 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| phenotype | dyslipidemia | “Specifically, VitD deficiency has been linked to an increased risk of dyslipidemia.” | 0.98 | phenotype_alias_lexicon_v2 |
| variant | rs10741657 | “In conclusion, our results suggest that rs10741657 G>A in CYP2R1 is associated with circulating LDL-C and HDL-C levels in a Lebanese cohort.” | 0.90 | hgvs_regex_v1 |
| gene | CYP2R1 | “However, the presence of the minor allele in rs10741657G>A of CYP2R1 was associated with increased levels in LDL-C (β = 4.95, p = 0.04)] and decreased levels in HDL-C (β = −1.76, p = 0.007)].” | 0.98 | hgnc_dict_v1 |