|
rs10830963
|
|
|
0.900 |
GeneticVariation |
BEFREE |
The common MTNR1B genetic variant rs10830963 is associated with an increased risk of type 2 diabetes (T2D).
|
26440713 |
2015 |
|
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 |
|
rs10830963
|
|
|
0.900 |
GeneticVariation |
BEFREE |
Two SNPs in melatonin receptor 1B gene, rs10830963 and rs1387153 showed significant associations with fasting plasma glucose levels and the risk of Type 2 Diabetes Mellitus (T2DM) in previous studies.
|
21658282 |
2011 |
|
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 |
|
rs10830963
|
|
|
0.900 |
GeneticVariation |
BEFREE |
The G-allele of MTNR1B rs10830963 increases risk of type 2 diabetes through a state of i-IFG and not through i-IGT.
|
19324940 |
2009 |
|
rs10830963
|
|
|
0.900 |
GeneticVariation |
BEFREE |
Our study shows that the diabetes risk variant rs10</span>830963 does not contribute to the known comorbidity between depression and type 2 diabetes.
|
30089436 |
2018 |
|
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 |
|
rs10830963
|
|
|
0.900 |
GeneticVariation |
BEFREE |
The association between late chronotype and higher risk of T2D appears to vary across MTNR1B rs10830963 genotypes.
|
31623012 |
2020 |
|
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 |