Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28362491
rs28362491
0.020 GeneticVariation BEFREE Therefore, our findings suggest that rs28362491 and rs5743708 polymorphisms were significantly associated with MO disease through acting by modulating serum CRP levels. 27507606

2016

dbSNP: rs28362491
rs28362491
0.020 GeneticVariation BEFREE Our results suggest that ins/ins genotype of SNP rs28362491 is linked to MO with high-level ALT, AST, ALP, and GGT. 29664665

2018

dbSNP: rs324420
rs324420
0.020 GeneticVariation BEFREE Our findings provide evidence for an endocannabinoid-related phenotype that may be identified by the combination of circulating anandamide levels with genotyping of the FAAH 385C>A; this phenotype is not exclusive to mono-ethnoracial populations nor to individuals with severe obesity. 26561012

2015

dbSNP: rs324420
rs324420
0.020 GeneticVariation BEFREE We were unable to find robust evidence of an association of the Pro129Thr</span> variant with severe obesity, and any related quantitative traits among the obese Greek subjects examined. 18819056

2008

dbSNP: rs4994
rs4994
0.020 GeneticVariation BEFREE To evaluate the prevalence of beta(3)-adrenergic receptor (ADRB3) Trp64Arg polymorphism and its relationship with the metabolic syndrome in severe obesity. 17299491

2007

dbSNP: rs4994
rs4994
0.020 GeneticVariation BEFREE Gender effect of the Trp64Arg mutation in the beta 3 adrenergic receptor gene on weight gain in morbid obesity. 9416435

1997

dbSNP: rs587777230
rs587777230
0.020 GeneticVariation BEFREE Interestingly, a morbid-obesity-associated R82* truncated mutant of CEP19 cannot ciliate nor interact with FOP and CEP350, indicative of a putative role for CEP19 in ciliopathies. 28659385

2017

dbSNP: rs587777230
rs587777230
0.020 GeneticVariation BEFREE Another truncating mutation p.Arg82* has been reported as responsible for morbid obesity in a family; however, in the family we present, not all homozygotes are obese, although some are severely obese. 29127258

2018

dbSNP: rs738409
rs738409
0.020 GeneticVariation BEFREE Morbid obesity exposes the association between PNPLA3 I148M (rs738409) and indices of hepatic injury in individuals of European descent. 19844213

2010

dbSNP: rs738409
rs738409
0.020 GeneticVariation BEFREE Aim of this study is to examine the relationship between PNPLA3 I148M genotypes and serum triglycerides, insulin resistance and T2D susceptibility by testing a gene-environment interaction model with severe obesity. 22724004

2012

dbSNP: rs10487818
rs10487818
0.010 GeneticVariation BEFREE One rare SNP, rs10487818, located in intron 4 of NAMPT was associated with severe obesity, with a minor allele frequency of 1.6% in controls, 0.4% in the class III obese adults and, remarkably, 0% in the severely obese children. 19300429

2009

dbSNP: rs1064891
rs1064891
0.010 GeneticVariation BEFREE Single nucleotide polymorphism rs1064891, located in the 3' UTR of the 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase 3 (PFKFB3) gene, was nominally associated with obesity in combined analysis of cohorts 1 and 2 (P=0.007) and, in men that were lean or had severe obesity, with BMI (P=or<0.005). 18180783

2008

dbSNP: rs121913564
rs121913564
0.010 GeneticVariation BEFREE Homozygous MC4R mutations, M161T and I316S, identified separately in 2 subjects (3.2%), were associated with severe obesity, hyperphagia, hyperleptinemia and hyperinsulinemia. 22463805

2012

dbSNP: rs121913566
rs121913566
0.010 GeneticVariation BEFREE N62S was found in homozygous form in five children with severe obesity from a consanguineous pedigree. 10903343

2000

dbSNP: rs12510549
rs12510549
0.010 GeneticVariation BEFREE Four single nucleotide polymorphisms within SLC2A9 (rs6855911, rs7442295, rs6449213, and rs12510549) were genotyped in the population-based prospective Bruneck Study (n = 800) and in a case-control study from Utah including 1,038 subjects recruited for severe obesity and 831 control subjects. 18487473

2008

dbSNP: rs1322837244
rs1322837244
0.010 GeneticVariation BEFREE Furthermore, both mutations PCSK1-p.Asn180Ser and POMC-p.Phe144Leu, which had previously been reported to be associated with severe obesity, were also identified in this study, but did not co-segregate with obesity. 24890885

2015

dbSNP: rs13447331
rs13447331
0.010 GeneticVariation BEFREE Overall, this study suggest that S127L may be the most frequent functional MC4R mutation leading to the severe obesity in general population and provides new insight into the functionality of population based variants of the MC4R. 24385306

2014

dbSNP: rs1799883
rs1799883
0.010 GeneticVariation BEFREE To investigate whether the Ala54Thr polymorphism of the fatty acid binding protein 2 gene is associated with obesity and obesity with dyslipidemia in Japanese schoolchildren, we analyzed 370 children with morbid obesity and 463 control children of normal weight. 11866034

2001

dbSNP: rs1800949
rs1800949
0.010 GeneticVariation BEFREE In conclusion, a previously unexplored ENPP1 haplotype composed of SNPs rs1800949 and rs943003 showed suggestive evidence for association with adult-onset morbid obesity in Finns. 18551113

2008

dbSNP: rs1801282
rs1801282
0.010 GeneticVariation BEFREE In this study, we investigated the association of PPAR-γ gene Pro12Ala (rs1801282) and C1431T (rs3856806) polymorphisms with morbid obesity and related phenotypes, in north Indian population. 22410809

2012

dbSNP: rs1805096
rs1805096
0.010 GeneticVariation BEFREE Our results suggest that rs1805134 polymorphism could be involved in the development of morbid obesity, whilst none of the alleles of the <i>LEPR</i> gene, rs1137100, rs1137101, rs1805094 and rs1805096 were associated as risk factors. 28096764

2016

dbSNP: rs1805097
rs1805097
0.010 GeneticVariation BEFREE These data indicate that IRS2 is an influential gene in severe obesity and glucose intolerance in this population, whereas gene-based haplotypes of IRS2 have revealed heterogeneity in the behaviour of the Gly1057Asp mutation in relation to insulin resistance. 12687350

2003

dbSNP: rs1805134
rs1805134
0.010 GeneticVariation BEFREE Our results suggest that rs1805134 polymorphism could be involved in the development of morbid obesity, whilst none of the alleles of the <i>LEPR</i> gene, rs1137100, rs1137101, rs1805094 and rs1805096 were associated as risk factors. 28096764

2016

dbSNP: rs1805192
rs1805192
0.010 GeneticVariation BEFREE In this study, we investigated the association of PPAR-γ gene Pro12Ala (rs1801282) and C1431T (rs3856806) polymorphisms with morbid obesity and related phenotypes, in north Indian population. 22410809

2012

dbSNP: rs199951903
rs199951903
CYTB ; ND6
0.010 GeneticVariation BEFREE The aim of this study was to evaluate whether the 15497 G/A mtDNA polymorphism (G251S) in the cytochrome b subunit of respiratory complex III, which has been associated with obesity-related variables and lipid metabolism in a Japanese population, is associated with severe obesity also in adult Caucasians from southern Italy. 17015183

2006