Advanced search

Combine gene, variant, phenotype, region and year filters

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.

Publications

3 records shown · first 60
TypeEntitySource evidenceConfidenceExtractor
variantrs2237892“The purpose of this study was to investigate the genes associated with β-cell dysfunction and their genetic roles in the rs7903146, rs2237892, and rs5219 variants in Saudi women diagnosed with type 2 diabetes mellitus and GDM.”0.90hgvs_regex_v1
geneTCF7L2“TCF7L2, KCNQ1, and KCNJ11 genes are connected to the mechanism of β-cell dysfunction.”0.98hgnc_dict_v1
geneKCNQ1“TCF7L2, KCNQ1, and KCNJ11 genes are connected to the mechanism of β-cell dysfunction.”0.98hgnc_dict_v1
geneKCNJ11“TCF7L2, KCNQ1, and KCNJ11 genes are connected to the mechanism of β-cell dysfunction.”0.98hgnc_dict_v1

Type 2 diabetes associated variants of KCNQ1 strongly confer the risk of cardiovascular disease among the Saudi Arabian population.

PMID 28863213 | PMCID PMC5596376 | DOI 10.1590/1678-4685-GMB-2017-0005 · Genetics and molecular biology · 2017 · 6 validated mentions
TypeEntitySource evidenceConfidenceExtractor
variantrs2237892“The current study was undertaken to evaluate the association of 3 polymorphisms of KCNQ1 (rs2237892, rs151290 and rs2237895) with T2D and/or CVD.”0.90hgvs_regex_v1
geneKCNQ1“Type 2 diabetes associated variants of KCNQ1 strongly confer the risk of cardiovascular disease among the Saudi Arabian population.”0.98hgnc_dict_v1
phenotypediabetes mellitus“Type 2 diabetes associated variants of KCNQ1 strongly confer the risk of cardiovascular disease among the Saudi Arabian population.”0.93phenotype_alias_lexicon_v2
populationSaudi Arabia“Type 2 diabetes associated variants of KCNQ1 strongly confer the risk of cardiovascular disease among the Saudi Arabian population. Patients diagnosed with either T2D (320 patients), CVD (250 patients) or both (60 patients) and 516 healthy controls were genotyped by TaqMan assay run on a real time PCR thermocycler.”0.95saudi_context_rules_v1

Association between FTO, MC4R, SLC30A8, and KCNQ1 gene variants and type 2 diabetes in Saudi population.

PMID 25501231 | DOI 10.4238/2014.December.4.14 · Genetics and molecular research : GMR · 2014 · 11 validated mentions
TypeEntitySource evidenceConfidenceExtractor
variantrs2237892“In the present study, we examined the association between variants in fat mass- and obesity-associated [rs9939609 (A/T)], melanocortin 4 receptor [rs17782313 (C/T), and rs12970134 (A/G)], SLC30A8 [rs13266634 (C/T)], and a member of the potassium voltage-gated channels [rs2237892(C/T)] genes in diabetes patients from Saudi Arabia.”0.90hgvs_regex_v1
geneFTO“Association between FTO, MC4R, SLC30A8, and KCNQ1 gene variants and type 2 diabetes in Saudi population.”0.98hgnc_dict_v1
geneMC4R“Association between FTO, MC4R, SLC30A8, and KCNQ1 gene variants and type 2 diabetes in Saudi population.”0.98hgnc_dict_v1
geneSLC30A8“Association between FTO, MC4R, SLC30A8, and KCNQ1 gene variants and type 2 diabetes in Saudi population.”0.98hgnc_dict_v1