Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4994
rs4994
0.020 GeneticVariation BEFREE Our results suggest that the Trp64Arg mutation is not a major determinant of metabolic disorders (type 2 diabetes, obesity) and chronic complications of type 2 diabetes in a Dutch population. 11213599

2001

dbSNP: rs1217691063
rs1217691063
0.010 GeneticVariation BEFREE The aim of this work was to evaluate the role of homocysteine, and the MTHFR 677C-->T allele as risk factors for premature coronary artery disease and to analyse the inheritance of this metabolic disorder. 11168435

2001

dbSNP: rs8192678
rs8192678
0.020 GeneticVariation BEFREE Our findings confirm that sex and age should be considered when investigating the influence of the PPARGC1A Gly482Ser polymorphism on metabolic disease. 16474966

2006

dbSNP: rs268
rs268
LPL
0.010 GeneticVariation BEFREE In addition, the relationships between the Asn291Ser variant and other metabolic diseases such as obesity and high blood pressure were also investigated in this systematic review. 16741292

2006

dbSNP: rs1801282
rs1801282
0.020 GeneticVariation BEFREE In conclusion, the PPARG Pro12Ala polymorphism might represent a genetic susceptibility factor for preterm birth and constitute a link between preterm birth and metabolic diseases later in life. 17259396

2007

dbSNP: rs1805192
rs1805192
0.010 GeneticVariation BEFREE In conclusion, the PPARG Pro12Ala polymorphism might represent a genetic susceptibility factor for preterm birth and constitute a link between preterm birth and metabolic diseases later in life. 17259396

2007

dbSNP: rs1917760
rs1917760
0.010 GeneticVariation BEFREE We investigated the association of SNP-1308G/T (rs1917760) of DsbA-L gene with metabolic diseases. 19225211

2009

dbSNP: rs738409
rs738409
0.040 GeneticVariation BEFREE The lack of a relationship with visceral obesity and the inverse correlation with CIMT suggest that fatty liver associated with the minor G allele of the PNPLA3 rs738409 polymorphism may not be linked to metabolic disorders. 20826584

2010

dbSNP: rs854560
rs854560
0.020 GeneticVariation BEFREE None of the variants of the Leu55Met PON1 polymorphism was associated with more frequent occurrence of PCOS or metabolic disorders, including insulin resistance. 20334584

2010

dbSNP: rs2016520
rs2016520
0.010 GeneticVariation BEFREE The objective of the study was to determine whether rs2016520 or other single-nucleotide polymorphism in the PPARD locus influenced the risk of developing various characteristics of metabolic disease. 20200337

2010

dbSNP: rs80356814
rs80356814
0.010 GeneticVariation BEFREE To determine the frequency distribution of LMNA 1908C>T SNP and its association with generalized obesity, abdominal obesity and coexistent metabolic disorders in nondiabetic Asian Indians living in a metropolitan city of north India. 21599722

2011

dbSNP: rs738409
rs738409
0.040 GeneticVariation BEFREE In Inter99, we analyzed associations of rs738409 with components of the WHO-defined metabolic syndrome (n = 5,847) and traits related to metabolic disease (n = 5,663). 22792295

2012

dbSNP: rs2241766
rs2241766
0.010 GeneticVariation BEFREE Adiponectin gene polymorphisms (T45G and G276T), adiponectin levels and risk for metabolic diseases in an Arab population. 22155316

2012

dbSNP: rs1799904
rs1799904
0.010 GeneticVariation BEFREE Our findings that this novel R80Q (rs1799904) variant both exhibits adverse effects on PC1/3 activity and is prevalent in the population suggests that further biochemical and genetic analysis to assess its contribution to the risk of metabolic disease within the general population is warranted. 23383060

2013

dbSNP: rs324420
rs324420
0.010 GeneticVariation BEFREE It has been demonstrated that the polymorphism 385 C/A of FAAH (fatty acid amide hydrolase) was associated with obesity and metabolic disorders. 22609216

2013

dbSNP: rs4986790
rs4986790
0.010 GeneticVariation BEFREE We observed a significant association between D299G polymorphism and metabolic disorders (T2DM and Met-S) risk (OR = 0.566, 95 % CI: 0.347-0.925, p = 0.023) particularly in Caucasians. 23275193

2013

dbSNP: rs4988235
rs4988235
0.010 GeneticVariation BEFREE Our aim was to test in this study, the association of rs4988235 with BMI and related metabolic diseases, in interaction with dairy product consumption. 23647908

2013

dbSNP: rs1801282
rs1801282
0.020 GeneticVariation BEFREE Thus, PPARγ2 rs1801282 polymorphism may play a significant role in the development of metabolic disorders in HIV/HCV coinfected patients, and might have an influence on the cardiovascular risk. 25159899

2014

dbSNP: rs11066280
rs11066280
0.010 GeneticVariation BEFREE Three gene variants, rs12229654, rs17249754, and rs11066280, were significantly associated with metabolic disorders such as hyperlipidemia and diabetes (P = 0.00071 to 0.0097, respectively). 24142389

2014

dbSNP: rs11635252
rs11635252
0.010 GeneticVariation BEFREE In conclusion, the CRTC3 polymorphism rs3862434 was associated with the plasma level of total cholesterol, and rs11635252 was associated with the risks of overweight and hypertriglyceridemia in a Chinese Han population, which might strengthen our understanding of the complex heredity of metabolic disorders. 24264430

2014

dbSNP: rs1431648262
rs1431648262
0.010 GeneticVariation BEFREE This perturbation in the desensitization-resensitization cycle of the GIPR variant, revealed in studies of cultured adipocytes, may contribute to the link of the E354Q variant to metabolic disease. 25047836

2014

dbSNP: rs17249754
rs17249754
0.010 GeneticVariation BEFREE Three gene variants, rs12229654, rs17249754, and rs11066280, were significantly associated with metabolic disorders such as hyperlipidemia and diabetes (P = 0.00071 to 0.0097, respectively). 24142389

2014

dbSNP: rs1799983
rs1799983
0.010 GeneticVariation BEFREE ESR1 XbaI and G894T NOS3 polymorphisms may be useful in accessing insulin resistance and type 2 diabetes risks in all women, even before menopause and occurrence of metabolic disease. 25077953

2014

dbSNP: rs267606841
rs267606841
0.010 GeneticVariation BEFREE Similarly, the prediction of high damaging behavior, evolutionary conservation and structural destabilization for C574G were proposed as major contributing factors to regulate metabolic disorder underlying tumor calcinosis and hyperostosis-hyperphosphatemia syndrome. 24038392

2014

dbSNP: rs3862434
rs3862434
0.010 GeneticVariation BEFREE In conclusion, the CRTC3 polymorphism rs3862434 was associated with the plasma level of total cholesterol, and rs11635252 was associated with the risks of overweight and hypertriglyceridemia in a Chinese Han population, which might strengthen our understanding of the complex heredity of metabolic disorders. 24264430

2014