Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10830963
rs10830963
0.900 GeneticVariation BEFREE The association between late chronotype and higher risk of T2D appears to vary across MTNR1B rs10830963 genotypes. 31623012

2020

dbSNP: rs10830963
rs10830963
0.900 GeneticVariation BEFREE While marginal evidence of interaction between self-reported morningness-eveningness preference and rs10830963 in risk of type 2 diabetes was seen, this interaction did not persist when analysis was expanded to include all participants regardless of employment status and when accelerometer-derived sleep midpoint was used as an objective measure of morningness-eveningness preference. 31757795

2020

dbSNP: rs10830963
rs10830963
0.900 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019

dbSNP: rs10830963
rs10830963
0.900 GeneticVariation BEFREE Our findings indicated that MTNR1B rs10830963 variant might serve as a genetic biomarker of T2DM, especially in South Asians. 30811895

2019

dbSNP: rs10830963
rs10830963
0.900 GeneticVariation BEFREE These data suggest that the <i>MTNR1B</i> rs10830963 and rs1387153 polymorphisms are associated with repaglinide monotherapy efficacy in Chinese patients with T2DM. 31787898

2019

dbSNP: rs10830963
rs10830963
G 0.900 GeneticVariation GWASCAT Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes. 30054458

2018

dbSNP: rs10830963
rs10830963
0.900 GeneticVariation BEFREE T2D risk was modeled using logistic regression with rs10830963 dosage, age, sex, and principal component as predictors. 29691896

2018

dbSNP: rs10830963
rs10830963
0.900 GeneticVariation BEFREE Our study shows that the diabetes risk variant rs10830963 does not contribute to the known comorbidity between depression and type 2 diabetes. 30089436

2018

dbSNP: rs10830963
rs10830963
G 0.900 GeneticVariation GWASCAT Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease. 28869590

2017

dbSNP: rs10830963
rs10830963
G 0.900 GeneticVariation GWASCAT Genetics of Type 2 Diabetes in U.S. Hispanic/Latino Individuals: Results From the Hispanic Community Health Study/Study of Latinos (HCHS/SOL). 28254843

2017

dbSNP: rs10830963
rs10830963
0.900 GeneticVariation BEFREE Among single-nucleotide polymorphisms mostly associated with T2D risk, rs10830963 is located in the MTNR1B gene, encoding one of the two receptors of melatonin, a neurohormone involved in circadian rhythms. 29063374

2017

dbSNP: rs10830963
rs10830963
0.900 GeneticVariation BEFREE Variants rs10830963 (C/G) and rs1387153 (C/T) in MTNR1B have been shown with an increased risk of developing type 2 diabetes and gestational diabetes mellitus. 26563312

2016

dbSNP: rs10830963
rs10830963
0.900 GeneticVariation BEFREE No associations between genetic variants of KLF14 rs972283, GCKR rs780094 or MTNR1B rs10830963 and T2DM were detected. 26927145

2016

dbSNP: rs10830963
rs10830963
0.900 GeneticVariation BEFREE The common MTNR1B genetic variant rs10830963 is associated with an increased risk of type 2 diabetes (T2D). 26440713

2015

dbSNP: rs10830963
rs10830963
0.900 GeneticVariation BEFREE Credible set variants were enriched for overlap with FOXA2 chromatin immunoprecipitation binding sites in human islet and liver cells, including at MTNR1B, where fine mapping implicated rs10830963 as driving T2D association. 26551672

2015

dbSNP: rs10830963
rs10830963
G 0.900 GeneticVariation GWASDB Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. 24509480

2014

dbSNP: rs10830963
rs10830963
G 0.900 GeneticVariation GWASCAT Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. 24509480

2014

dbSNP: rs10830963
rs10830963
0.900 GeneticVariation BEFREE Among Caucasian women, GDM was associated with carriage of TCF7L2 rs7901695, MTNR1B rs10830963 and GCKR rs780094 alleles that are associated with T2DM and fasting glucose in nonpregnant populations. 23456907

2014

dbSNP: rs10830963
rs10830963
0.900 GeneticVariation BEFREE An association of the MTNR1B variant rs10830963 with T2D risk was not detected in our cohort. 24710643

2014

dbSNP: rs10830963
rs10830963
0.900 GeneticVariation BEFREE Variants in the KCNQ1 (rs2237895, p = 0.0012), HHEX (rs1111875, p = 0.0024 in Finns) and MTNR1B (rs10830963, p = 0.0039) loci showed the strongest association in patients with low GADA, supporting the hypothesis that the disease in these patients is more like type 2 diabetes. 24906951

2014

dbSNP: rs10830963
rs10830963
0.900 GeneticVariation BEFREE Overall, the pooled results indicated that GCK (rs1799884), GCKR (rs780094) and MTNR1B (rs10830963) were significantly associated with T2DM susceptibility (OR, 1.04; 95%CI, 1.01-1.08; OR, 1.08; 95%CI, 1.05-1.12 and OR, 1.05; 95%CI, 1.02-1.08, respectively). 23840762

2013

dbSNP: rs10830963
rs10830963
G 0.900 GeneticVariation GWASCAT Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes. 22885922

2012

dbSNP: rs10830963
rs10830963
0.900 GeneticVariation BEFREE Two common variants (rs1387153, rs10830963) in MTNR1B have been reported to have independent effects on fasting blood glucose (FBG) levels with increased risk to type 2 diabetes (T2D) in recent genome-wide association studies (GWAS). 21558052

2012

dbSNP: rs10830963
rs10830963
0.900 GeneticVariation BEFREE To examine the association of type 2 diabetes susceptibility loci and visceral fat accumulation, we genotyped 1279 Japanese subjects (556 men and 723 women), who underwent computed tomography for measurements of visceral fat area (VFA) and subcutaneous fat area (SFA) for the following single-nucleotide polymorphisms (SNPs): NOTCH2 rs10923931, THADA rs7578597, PPARG rs1801282, ADAMTS9 rs4607103, IGF2BP2 rs1470579, VEGFA rs9472138, JAZF1 rs864745, CDKN2A/CDKN2B rs564398 and rs10811661, HHEX rs1111875 and rs5015480, TCF7L2 rs7901695, KCNQ1 rs2237892, KCNJ11 rs5215 and rs5219, EXT2 rs1113132, rs11037909, and rs3740878, MTNR1B rs10830963, DCD rs1153188, TSPAN8/LGR5 rs7961581, and FTO rs8050136 and rs9939609. 22377712

2012

dbSNP: rs10830963
rs10830963
0.900 GeneticVariation BEFREE We analyzed nine single-nucleotide polymorphisms (SNPs), including rs340874 (PROX1), rs4607517 (GCK), rs2191349 (DGKB-TMEM195), rs7034200 (GLIS3), rs10885122 (ADRA2A), rs174550 (FADS1), rs11605924 (CRY2), rs10830963 (MTNR1B) and rs35767 (IGF1). rs340874 (PROX1) and rs174550 (FADS1) were significantly associated with T2D (P=0.0078, OR: 1.12; and P=0.0071, OR: 1.12, respectively). 22992776

2012