Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7754840
rs7754840
0.890 GeneticVariation BEFREE We assessed associations of GDM related genetic variants in/near the CDKAL1 (rs7754840) and MTNR1B (rs10830962) genes with changes in fasting levels of glucose and insulin, β-cell function (HOMA-B) and insulin resistance (HOMA-IR) at 1 year and 2 years after the baseline. 31542245

2019

dbSNP: rs7754840
rs7754840
0.890 GeneticVariation BEFREE Our meta-analysis showed that two SNPs in particular(rs7754840 and rs7756992 in CDKAL1) were very strongly associated with GDM risk. 30074065

2018

dbSNP: rs7754840
rs7754840
0.890 GeneticVariation BEFREE The most important risk alleles associated with GDM were rs10830963/G of MTNR1B (OR = 1.84/1.64 [IADPSG/m'99WHO], p = 0.0007/0.006), rs7754840/C (OR = 1.51/NS, p = 0.016) of CDKAL1 and rs1799884/T (OR = 1.4/1.56, p = 0.04/0.006) of GCK. 28072873

2017

dbSNP: rs7754840
rs7754840
0.890 GeneticVariation BEFREE The rs7754840 and rs7756992 SNPs of the CDKAL1 gene were found to be associated with GDM in this south Indian population. 25723968

2015

dbSNP: rs7754840
rs7754840
0.890 GeneticVariation BEFREE The minor alleles of rs7903146 (TCF7L2), rs12255372 (TCF7L2), rs1799884 (-30G/A, GCK), rs5219 (E23K, KCNJ11), rs7754840 (CDKAL1), rs4402960 (IGF2BP2), rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs1801278 (Gly972Arg, IRS1) were significantly associated with a higher risk of GDM. 23690305

2013

dbSNP: rs7754840
rs7754840
0.890 GeneticVariation BEFREE These polymorphisms were in or near the following genes: TCF7L2 (rs7903146), MTNR1B (rs10830963), IGF2BP2 (rs4402960), KCNJ11 (rs5219), CDKAL1 (rs7754840), KCNQ1 (rs2237892 and rs2237895) and GCK (rs4607517); while no association was found for PPARG with GDM risk. 23029294

2012

dbSNP: rs7754840
rs7754840
0.890 GeneticVariation BEFREE Two loci known to be associated with type 2 diabetes had a genome-wide significant association with GDM in the joint analysis. rs7754840, a variant in CDKAL1, had the strongest association with GDM (odds ratio 1.518; P=6.65×10(-16)). 22233651

2012

dbSNP: rs7754840
rs7754840
0.890 GeneticVariation BEFREE We also found that the risk alleles of rs2383208 (b = -0.085, p = 0.003), rs4402960 (b = -0.057, p = 0.046) and rs10830963 (b = -0.096, p = 0.001) were associated with HOMA-B, while rs7754840 was associated with decrease in insulin AUC during a 100 g OGTT given at the time of GDM diagnosis (b = -0.080, p = 0.007). 22096510

2011

dbSNP: rs7754840
rs7754840
0.890 GeneticVariation BEFREE Compared with controls (men and women combined), GDM</span> was associated with rs7756992 and rs7754840 (OR 1.55, 95% CI 1.34-1.79, p = 4.17 x 10(-9)) in CDKAL1; rs10811661 (OR 1.49, 95% CI 1.29-1.72, p = 1.05 x 10(-7)) in the CDKN2A-CDKN2B region; rs1111875 (OR 1.27, 95% CI 1.09-1.49, p = 0.003), rs5015480, and rs7923837 in HHEX; rs4402960 (OR 1.18, 95% CI 1.01-1.38, p = 0.03) in IGF2BP2; rs13266634 (OR 1.24, 95% CI 1.07-1.43, p = 0.005) in SLC30A8; and rs7903146 (OR 1.58, 95% CI 1.03-2.43, p = 0.038) in TCF7L2. 19002430

2009

dbSNP: rs10830962
rs10830962
0.840 GeneticVariation BEFREE Association of rs10830962 polymorphism with gestational diabetes mellitus risk in a Chinese population. 30926842

2019

dbSNP: rs10830962
rs10830962
0.840 GeneticVariation BEFREE We assessed associations of GDM related genetic variants in/near the CDKAL1 (rs7754840) and MTNR1B (rs10830962) genes with changes in fasting levels of glucose and insulin, β-cell function (HOMA-B) and insulin resistance (HOMA-IR) at 1 year and 2 years after the baseline. 31542245

2019

dbSNP: rs10830962
rs10830962
0.840 GeneticVariation BEFREE The rs10830962 polymorphism in MTNR1B was not associated with an increased risk of developing GDM or any of the clinical or metabolic characteristics in patients with GDM (p > 0.05). 24157813

2013

dbSNP: rs10830962
rs10830962
0.840 GeneticVariation BEFREE A variant near MTNR1B, rs10830962, was also significantly associated with the risk of GDM (1.454; P=2.49×10(-13)). 22233651

2012

dbSNP: rs10830963
rs10830963
0.100 GeneticVariation BEFREE FPRP and TSA analyses confirmed findings support that the rs10830963 G allele increases the risk of GDM, and further functional experimental studies are warranted to explore and clarify the potential mechanism. 31808503

2019

dbSNP: rs10830963
rs10830963
0.100 GeneticVariation BEFREE Furthermore, rs10830963 may tag a molecular mechanism leading to insulin resistance in Han Chinese women with GDM. 29656698

2019

dbSNP: rs10830963
rs10830963
0.100 GeneticVariation BEFREE Our findings indicated that <i>MTNR1B</i> rs1387153, rs4753426, and rs10830963 variants might serve as genetic biomarkers of GDM. 30991439

2019

dbSNP: rs10830963
rs10830963
0.100 GeneticVariation BEFREE The findings of this study suggest that rs10830963 and rs7936247 may be markers for susceptibility to GDM in a Chinese population. 30912250

2019

dbSNP: rs7903146
rs7903146
0.100 GeneticVariation BEFREE These results provide evidence that the T risk allele in TCF7L2 rs7903146 is associated with failure in early postprandial glycemic control and requirement of insulin therapy in women with gestational diabetes mellitus, even after adjusting for confounding factors such BMI and age. 31546272

2019

dbSNP: rs10830963
rs10830963
0.100 GeneticVariation BEFREE The established circadian rhythm-associated MTNR1B genetic variant (rs10830963) was genotyped in 1025 Chinese women with a history of GDM. 29590381

2018

dbSNP: rs10830963
rs10830963
0.100 GeneticVariation BEFREE Carrying the <i>MTNR1B</i> rs10830963/<i>G</i> risk allele-in interaction with pre-pregnancy BMI-is likely be considered as a candidate pharmacogenetic marker of antenatal insulin therapy initiation and should be further assessed in precision medicine trials in GDM. 30477160

2018

dbSNP: rs10830963
rs10830963
0.100 GeneticVariation BEFREE In addition, we confirmed three variants, rs10830963 (MTNR1B), rs1387153 (MTNR1B) and rs4506565 (TCF7L2), that had previously been significantly associated with GDM risk. 29947923

2018

dbSNP: rs1801282
rs1801282
0.100 GeneticVariation BEFREE The rs1801282 polymorphism may not be associated with genetic susceptibility to GDM in whites. 29885389

2018

dbSNP: rs7903146
rs7903146
0.100 GeneticVariation BEFREE However, the additional presence of TCF7L2 rs7903146 risk alleles does not further aggravate the negative impact of a history of gestational diabetes on metabolic traits related to T2DM. 30419301

2018

dbSNP: rs7903146
rs7903146
0.100 GeneticVariation BEFREE The genetic variant rs7903146 (C > T) in TCF7L2 gene showed a strong association with GDM risk (OR: 2.56; 95% CI: [1.24-5.29]). 29325775

2018

dbSNP: rs7903146
rs7903146
0.100 GeneticVariation BEFREE For the first time, we identified eight variants associated with GDM, namely rs7957197 (HNF1A), rs10814916 (GLIS3), rs3802177 (SLC30A8), rs9379084 (RREB1), rs34872471 (TCF7L2), rs7903146 (TCF7L2), rs11787792 (GPSM1) and rs7041847 (GLIS3). 29947923

2018