Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1333049
rs1333049
CDKN2B-AS1
0.740 GeneticVariation BEFREE Genotype CC of rs1333049 was significantly associated with both elevated CRP levels and decreased HDL concentrations after univariate (p = 0.028, p = 0.012) and multivariate analysis (p = 0.041, p = 0.023) stratified for age, gender, body mass index, smoking, diabetes, and severe periodontitis. 31770616

2020
dbSNP: rs13266634
rs13266634
SLC30A8 ; LOC105375716
0.100 GeneticVariation BEFREE Polymorphism rs13266634 in SLC30A8 causes abnormal synthesis, maturation and secretion of insulin, resulting in decrease in efficiency of glucose metabolism and diabetes. 30633652

2020
dbSNP: rs7903146
rs7903146
TCF7L2
0.100 GeneticVariation BEFREE There is a trend toward an association between faster GE and the diabetes-associated allele at rs7903146 in TCF7L2. 31691451

2020
dbSNP: rs28938469
rs28938469
ABCC8
0.010 GeneticVariation BEFREE We explored the gene responsible for diabetes in two brothers, who were suspected to have diabetes </span>at 15 and 18 years-of-age, respectively, with whole exome sequencing, and identified a compound heterozygous ABCC8 gene mutation (p.Arg168Cys and p.Arg1421Cys). 31479591

2020
dbSNP: rs36217263
rs36217263
KL
0.010 GeneticVariation BEFREE The deletion of at least one copy of allele A of rs36217263 near Klotho showed statistically significant association with poor response to beta-blockers (dominant; odds ratio (OR) = 3.89; P = 0.017), adjusted for diabetes and dyslipidemia. 31350855

2020
dbSNP: rs505151
rs505151
PCSK9
0.010 GeneticVariation BEFREE In CAD patients, the AG genotype of PSCK9 rs505151 is associated with diabetes and a positive family history of CAD. 30947598

2020
dbSNP: rs756823374
rs756823374
ABCC8
0.010 GeneticVariation BEFREE We explored the gene responsible for diabetes in two brothers, who were suspected to have diabetes at 15 and 18 years-of-age, respectively, with whole exome sequencing, and identified a compound heterozygous ABCC8 gene mutation (p.Arg168Cys and p.Arg1421Cys). 31479591

2020
dbSNP: rs8133052
rs8133052
CBR3 ; CBR3-AS1
0.010 GeneticVariation BEFREE Regarding the docetaxel phase, high levels of abdominal pain and mucositis were related to CBR3 gene (rs8133052) polymorphism and diabetes respectively. 31056713

2020
dbSNP: rs9939609
rs9939609
FTO
0.800 GeneticVariation BEFREE Diabetes genomics research has illuminated single nucleotide polymorphism (SNP) in several genes including, fat mass and obesity associated (FTO) (rs9939609 and rs9926289), potassium voltage-gated channel subfamily J member 11 (rs5219), SLC30A 8 (rs13266634) and peroxisome proliferator-activated receptor gamma 2 (rs1805192). 31823921

2019
dbSNP: rs9939609
rs9939609
FTO
0.800 GeneticVariation BEFREE Additionally, both omentin Val109Asp and FTO rs9939609 polymorphisms were significantly positively correlated to familial history of diabetes (P = 0.046 and P = 0.024, respectively). 31200723

2019
dbSNP: rs1333049
rs1333049
CDKN2B-AS1
0.740 GeneticVariation BEFREE For CHD patients, rs1333049 decreased the risk of diabetes under heterozygote (p = .014) and dominant (p = .024) models. 31496134

2019
dbSNP: rs10084572
rs10084572
LOC105372829
T 0.700 GeneticVariation GWASCAT Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. 31451708

2019
dbSNP: rs10224210
rs10224210
PRKAG2
T 0.700 GeneticVariation GWASCAT Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. 31451708

2019
dbSNP: rs1047891
rs1047891
CPS1
A 0.700 GeneticVariation GWASCAT Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. 31451708

2019
dbSNP: rs10941191
rs10941191 		A 0.700 GeneticVariation GWASCAT Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. 31451708

2019
dbSNP: rs1264347
rs1264347
LINC00243
T 0.700 GeneticVariation GWASCAT Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. 31451708

2019
dbSNP: rs12922822
rs12922822
UMOD
T 0.700 GeneticVariation GWASCAT Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. 31451708

2019
dbSNP: rs13146355
rs13146355
SHROOM3
A 0.700 GeneticVariation GWASCAT Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. 31451708

2019
dbSNP: rs13191445
rs13191445 		A 0.700 GeneticVariation GWASCAT Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. 31451708

2019
dbSNP: rs145590578
rs145590578
SLC22A2
A 0.700 GeneticVariation GWASCAT Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. 31451708

2019
dbSNP: rs149131600
rs149131600
HPN ; HPN-AS1
T 0.700 GeneticVariation GWASCAT Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria. 31511532

2019
dbSNP: rs1556751
rs1556751
PIP5K1B
A 0.700 GeneticVariation GWASCAT Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. 31451708

2019
dbSNP: rs17137004
rs17137004
FOXP2
A 0.700 GeneticVariation GWASCAT Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria. 31511532

2019
dbSNP: rs1906436
rs1906436
WDR72
T 0.700 GeneticVariation GWASCAT Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. 31451708

2019
dbSNP: rs200950799
rs200950799 		T 0.700 GeneticVariation GWASCAT Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. 31451708

2019