Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17381664
rs17381664
C 0.800 GeneticVariation GWASDB Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. 23563607

2013

dbSNP: rs17381664
rs17381664
C 0.800 GeneticVariation GWASCAT Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. 23563607

2013

dbSNP: rs774006043
rs774006043
0.010 GeneticVariation BEFREE Similarly, LEPR 668 A/G + G/G carriers with a high fat total intake had 3.0 times higher risk of obesity (p = 0.002) and 4.1 times higher risk of hypercholesterolemia (p = 0.001). 26365669

2015

dbSNP: rs778114184
rs778114184
0.010 GeneticVariation BEFREE Here we show that the Arg282Ser mutation in APOA5 gene is associated with a significant reduction of TG (-15.5 mg/dl), total (-18.1 mg/dl) and LDL-cholesterol (-14.8 mg/dl) levels in overweight/obese children and adolescents, indicating that indeed this association appears early in life. 28927406

2017

dbSNP: rs2047937
rs2047937
0.010 GeneticVariation BEFREE We identified seven potentially pleiotropic loci-rs3759579 (MARK3), rs2178950 (TRPS1), rs1473 (PUM1), rs9825174 (XXYLT1), rs2047937 (ZNF423), rs17277372 (DNM3), and rs335170 (PRDM6)-associated with osteoporosis and obesity. 29145611

2018

dbSNP: rs9825174
rs9825174
0.010 GeneticVariation BEFREE We identified seven potentially pleiotropic loci-rs3759579 (MARK3), rs2178950 (TRPS1), rs1473 (PUM1), rs9825174 (XXYLT1), rs2047937 (ZNF423), rs17277372 (DNM3), and rs335170 (PRDM6)-associated with osteoporosis and obesity. 29145611

2018

dbSNP: rs1799782
rs1799782
0.010 GeneticVariation BEFREE The C allele of rs861539 and T allele of rs1799782 Interaction between rs1799782 and obesity and haplotype T- C were all associated with increased PTC risk. 30165355

2018

dbSNP: rs25487
rs25487
0.010 GeneticVariation BEFREE We uncovered a significant association between obesity (body mass index, ≥ 25) and rs25487. 24172093

2013

dbSNP: rs9923451
rs9923451
0.800 GeneticVariation GWASDB A genome-wide association study on obesity and obesity-related traits. 21552555

2011

dbSNP: rs9923451
rs9923451
0.800 GeneticVariation GWASCAT A genome-wide association study on obesity and obesity-related traits. 21552555

2011

dbSNP: rs35034312
rs35034312
0.010 GeneticVariation BEFREE Three other rare missense variants were found in obese probands, but these did not clearly cosegregate with obesity in family studies and one (P301S), which was found in three unrelated subjects with early-onset obesity, had normal functional properties. 16477437

2006

dbSNP: rs553395822
rs553395822
0.010 GeneticVariation BEFREE R228Q was the only coding, non-synonymous variant that was exclusively found in patients, but the variant did not co-segregate with obesity in the three investigated siblings. 23104151

2013

dbSNP: rs10010131
rs10010131
0.010 GeneticVariation BEFREE Polymorphisms in TCF7L2 (rs7903146, OR 1.10, 95% CI 1.04-1.17, p = 0.00097), FTO (rs9939609, OR 1.08, 95% CI 1.02-1.14, p = 0.0065), WFS1 (rs10010131, OR 1.07, 95% CI 1.02-1.13, p = 0.0078) and IGF2BP2 (rs4402960, OR 1.07, 95% CI 1.01-1.13, p = 0.021) predicted the development of at least three components of the metabolic syndrome in both univariate and multivariate analysis; in the case of TCF7L2, WFS1 and IGF2BP this was due to their association with hyperglycaemia (p < 0.00001, p = 0.0033 and p = 0.027, respectively) and for FTO it was due to its association with obesity (p = 0.004). 18853134

2008

dbSNP: rs2441666
rs2441666
0.010 GeneticVariation BEFREE Only FTO rs9939609 A>T polymorphism was associated with obesity and no association was observed with ADIPOQ rs2441666 G>T and ACE rs4340288 DIP. 30416093

2019

dbSNP: rs1802295
rs1802295
0.020 GeneticVariation BEFREE The aim of the current study was to analyze the effect of six type II diabetes GWAS loci rs3923113 (GRB14), rs16861329 (ST6GAL1), rs1802295 (VPS26A), rs7178572 (HMG20A), rs2028299 (AP3S2) and rs4812829 (HNF4A), and an FTO polymorphism (rs9939609) on obesity. 26395551

2016

dbSNP: rs1802295
rs1802295
0.020 GeneticVariation BEFREE MAF of G2548A was 42.8% in obese and 30.1% in controls (<i>P</i>=5.7 × 10<sup>-5</sup>), it showed association with weight, body mass index (BMI), waist circumference (WC), high density lipoprotein cholesterol (HDL-c) and leptin, Gln223Arg had MAF 32% in obese and 18.7% in controls (<i>P</i>=5.4 × 10<sup>-6</sup>), it showed association with fasting plasma glucose (FPG) and all lipid traits, Ala54Thr had MAF 42.4% in obese and 33.1% (<i>P</i>=0.002), it showed association with none of the tested parameters. rs9939609 MAF was 26.6%, and showed association with none of the tested parameters. rs1802295 (<i>P</i>=0.002); rs7178572 (<i>P</i>=0.007); rs2028299 (<i>P</i>=0.04); rs4812829 (<i>P</i>=0.02) showed significant while rs3923113 and rs16861329 did not show a significant association (<i>P</i>=0.20 and <i>P</i>=0.3, respectively) with obesity. 29752338

2018

dbSNP: rs35400704
rs35400704
VGF
0.010 GeneticVariation BEFREE To assess the functional equivalence of human VGF(1-615) (hVGF) and mouse VGF(1-617) (mVGF), and to elucidate the function of the VGF C-terminal region in the regulation of energy balance and susceptibility to obesity, we generated humanized VGF knockin mouse models expressing full-length hVGF or a C-terminally deleted human VGF(1-524) (hSNP), encoded by a single nucleotide polymorphism (rs35400704). 25675362

2015

dbSNP: rs752907384
rs752907384
0.010 GeneticVariation BEFREE The ACE I/D, AT2 C3123A, TGF-β1 T869C, and VEGF T460C polymorphisms can affect susceptibility to obesity or overweight in Korean children. 29115082

2017

dbSNP: rs1544410
rs1544410
VDR
0.030 GeneticVariation BEFREE The rs1544410 or BsmI single nucleotide polymorphism (SNP) in the intronic region of the VDR gene has been previously associated with vitamin D levels, obesity and insulin resistance. 28617856

2017

dbSNP: rs1544410
rs1544410
VDR
0.030 GeneticVariation BEFREE Results showed that the VDR SNPs rs731236 (G) (TaqI) and rs1544410 (T) (Bsm-I) minor allele polymorphisms are significantly more frequent in obese individuals (p = 0.009, β = 0.086 and p = 0.028, β = 0.072, respectively). 25020064

2014

dbSNP: rs1544410
rs1544410
VDR
0.030 GeneticVariation BEFREE The aim of this study was to investigate the association of candidate gene single nucleotide polymorphisms (SNPs), namely FTO (rs9939609) and VDR (rs1544410), with obesity in the UAE population. 29343214

2018

dbSNP: rs731236
rs731236
VDR
0.020 GeneticVariation BEFREE Analysis of vitamin D receptor (VDR) TaqI (rs731236; T/C) and fat mass and obesity-associated (FTO) (rs9939609; A/T) [corrected] polymorphisms in 82 obesity subjects and 102 controls showed significant association for VDR TaqI 'T' allele and obesity (OR: 2.07; 1.123-3.816; P=0.019), contributing to an elevated BMI of 3kg/m(2) per risk allele. 23103831

2013

dbSNP: rs731236
rs731236
VDR
0.020 GeneticVariation BEFREE Results showed that the VDR SNPs rs731236 (G) (TaqI) and rs1544410 (T) (Bsm-I) minor allele polymorphisms are significantly more frequent in obese individuals (p = 0.009, β = 0.086 and p = 0.028, β = 0.072, respectively). 25020064

2014

dbSNP: rs12721377
rs12721377
VDR
0.010 GeneticVariation BEFREE Therefore, polymorphisms in the GC (rs2282679, rs4588, rs7041) and VDR (rs12721377) genes were independently associated with obesity and 25OHD3 levels with a clear sex dimorphism. 26881316

2016

dbSNP: rs2239179
rs2239179
VDR
0.010 GeneticVariation BEFREE Interactions between two previously studied VDR polymorphisms (rs7968585 and rs2239179) and 25OHD concentrations on metabolic and cardiovascular disease-related outcomes such as obesity- (body mass index, waist circumference, waist-hip ratio (WHR)), cardiovascular- (systolic and diastolic blood pressure), lipid- (high- and low-density lipoprotein, triglycerides, total cholesterol), inflammatory- (C-reactive protein, fibrinogen, insulin growth factor-1, tissue plasminogen activator) and diabetes- (glycated haemoglobin) related markers were examined in the 1958 British Birth cohort (n up to 5160). 24582179

2014