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VDR and metabolic syndrome are reported together in 2 articles.

Gene

VDR

HGNC
HGNC:12679
87articles
87mentions
10variants with confirmed gene link (top 10)
Most co-reported phenotypes (articles)
Reported variants (articles · ClinVar status)
141articles
141mentions
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

2 records shown · first 60

The Association Between FokI Vitamin D Receptor Polymorphisms With Metabolic Syndrome Among Pregnant Arab Women.

PMID 35282461 | PMCID PMC8909137 | DOI 10.3389/fendo.2022.844472 · Frontiers in endocrinology · 2022 · 3 validated mentions
TypeEntitySource evidenceConfidenceExtractor
geneVDR“The link between vitamin D receptor (VDR) gene polymorphisms and maternal MetS has been observed in several ethnic groups, but is yet to be clarified in the Arabian population.”0.98hgnc_dict_v1
phenotypemetabolic syndrome“The Association Between FokI Vitamin D Receptor Polymorphisms With Metabolic Syndrome Among Pregnant Arab Women.”0.98phenotype_alias_lexicon_v2
populationSaudi Arabia“Metabolic syndrome (MetS) is a serious health condition that is becoming extremely threatening in Saudi Arabia. This study aims to investigate the relationship between the FokI VDR genotype and the risk of MetS and its components in pregnant Saudi women. A cross-sectional study was conducted using 368 pregnant Saudi women on first trimester screened for MetS (44 with MetS and 324 without MetS).”0.95saudi_context_rules_v1
TypeEntitySource evidenceConfidenceExtractor
geneVDR“This study was conducted to assess the association between vitamin D receptor (VDR) polymorphisms and genetic susceptibility to components of the metabolic syndrome, type 2 diabetes mellitus (T2DM), and vitamin D deficiency in the Saudi Arabian population.”0.98hgnc_dict_v1
phenotypemetabolic syndrome“Association of VDR-gene variants with factors related to the metabolic syndrome, type 2 diabetes and vitamin D deficiency.”0.98phenotype_alias_lexicon_v2
phenotypeobesity“The CT genotype and allele T of BsmI were associated with lower HDL-C levels [OR 0.60 (0.37, 0.96), p=0.03] and obesity [OR 1.4 (1.0, 1.90), p=0.04], respectively.”0.98phenotype_alias_lexicon_v2
phenotypediabetes mellitus“Association of VDR-gene variants with factors related to the metabolic syndrome, type 2 diabetes and vitamin D deficiency.”0.93phenotype_alias_lexicon_v2