SLC2A2, solute carrier family 2 member 2, 6514

N. diseases: 123; N. variants: 32
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11920090
rs11920090
Entrez Id: 6514
Gene Symbol: SLC2A2
SLC2A2
CUI: C0428568
Disease:
Fasting blood glucose measurement 		A 0.800 GeneticVariation GWASCAT Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility. 25631608 2015
dbSNP: rs11920090
rs11920090
Entrez Id: 6514
Gene Symbol: SLC2A2
SLC2A2
CUI: C1305855
Disease:
Body mass index 		A 0.800 GeneticVariation GWASCAT A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance. 22581228 2012
dbSNP: rs11920090
rs11920090
Entrez Id: 6514
Gene Symbol: SLC2A2
SLC2A2
CUI: C0428568
Disease:
Fasting blood glucose measurement 		0.800 GeneticVariation GWASDB Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways. 22885924 2012
dbSNP: rs11920090
rs11920090
Entrez Id: 6514
Gene Symbol: SLC2A2
SLC2A2
CUI: C1305855
Disease:
Body mass index 		0.800 GeneticVariation GWASDB A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance. 22581228 2012
dbSNP: rs11920090
rs11920090
Entrez Id: 6514
Gene Symbol: SLC2A2
SLC2A2
CUI: C0428568
Disease:
Fasting blood glucose measurement 		A 0.800 GeneticVariation GWASCAT A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance. 22581228 2012
dbSNP: rs10513686
rs10513686
Entrez Id: 6514
Gene Symbol: SLC2A2
SLC2A2
CUI: C1278049
Disease:
Serum gamma-glutamyl transferase measurement 		A 0.800 GeneticVariation GWASDB Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma. 22001757 2011
dbSNP: rs10513686
rs10513686
Entrez Id: 6514
Gene Symbol: SLC2A2
SLC2A2
CUI: C1278049
Disease:
Serum gamma-glutamyl transferase measurement 		A 0.800 GeneticVariation GWASCAT Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma. 22001757 2011
dbSNP: rs11920090
rs11920090
Entrez Id: 6514
Gene Symbol: SLC2A2
SLC2A2
CUI: C0428568
Disease:
Fasting blood glucose measurement 		T 0.800 GeneticVariation GWASCAT New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. 20081858 2010
dbSNP: rs121909744
rs121909744
Entrez Id: 6514
Gene Symbol: SLC2A2
SLC2A2
CUI: C3495427
Disease:
Fanconi-Bickel Syndrome 		0.800 GeneticVariation UNIPROT Mutation analysis of the GLUT2 gene in patients with Fanconi-Bickel syndrome. 11044475 2000
dbSNP: rs121909747
rs121909747
Entrez Id: 6514
Gene Symbol: SLC2A2
SLC2A2
CUI: C3495427
Disease:
Fanconi-Bickel Syndrome 		0.800 GeneticVariation UNIPROT Mutation analysis of the GLUT2 gene in patients with Fanconi-Bickel syndrome. 11044475 2000
dbSNP: rs28928874
rs28928874
Entrez Id: 6514
Gene Symbol: SLC2A2
SLC2A2
CUI: C3495427
Disease:
Fanconi-Bickel Syndrome 		0.800 GeneticVariation UNIPROT Mutation analysis of the GLUT2 gene in patients with Fanconi-Bickel syndrome. 11044475 2000
dbSNP: rs121909744
rs121909744
Entrez Id: 6514
Gene Symbol: SLC2A2
SLC2A2
CUI: C3495427
Disease:
Fanconi-Bickel Syndrome 		0.800 GeneticVariation UNIPROT A mutation in GLUT2, not in phosphorylase kinase subunits, in hepato-renal glycogenosis with Fanconi syndrome and low phosphorylase kinase activity. 10987651 1999
dbSNP: rs121909747
rs121909747
Entrez Id: 6514
Gene Symbol: SLC2A2
SLC2A2
CUI: C3495427
Disease:
Fanconi-Bickel Syndrome 		0.800 GeneticVariation UNIPROT A mutation in GLUT2, not in phosphorylase kinase subunits, in hepato-renal glycogenosis with Fanconi syndrome and low phosphorylase kinase activity. 10987651 1999
dbSNP: rs28928874
rs28928874
Entrez Id: 6514
Gene Symbol: SLC2A2
SLC2A2
CUI: C3495427
Disease:
Fanconi-Bickel Syndrome 		0.800 GeneticVariation UNIPROT A mutation in GLUT2, not in phosphorylase kinase subunits, in hepato-renal glycogenosis with Fanconi syndrome and low phosphorylase kinase activity. 10987651 1999
dbSNP: rs121909744
rs121909744
Entrez Id: 6514
Gene Symbol: SLC2A2
SLC2A2
CUI: C3495427
Disease:
Fanconi-Bickel Syndrome 		A 0.800 CausalMutation CLINVAR
dbSNP: rs121909747
rs121909747
Entrez Id: 6514
Gene Symbol: SLC2A2
SLC2A2
CUI: C3495427
Disease:
Fanconi-Bickel Syndrome 		G 0.800 CausalMutation CLINVAR
dbSNP: rs28928874
rs28928874
Entrez Id: 6514
Gene Symbol: SLC2A2
SLC2A2
CUI: C3495427
Disease:
Fanconi-Bickel Syndrome 		T 0.800 CausalMutation CLINVAR
dbSNP: rs8192675
rs8192675
Entrez Id: 6514
Gene Symbol: SLC2A2
SLC2A2
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		0.710 GeneticVariation BEFREE The variant rs8192675 in the SLC2A2 gene (C allele) is associated with an improved glucose response to metformin monotherapy during the first year after diagnosis in type 2 diabetes. 30413829 2019
dbSNP: rs8192675
rs8192675
Entrez Id: 6514
Gene Symbol: SLC2A2
SLC2A2
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		T 0.710 GeneticVariation GWASCAT An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans. 28566273 2017
dbSNP: rs8192675
rs8192675
Entrez Id: 6514
Gene Symbol: SLC2A2
SLC2A2
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		C 0.710 GeneticVariation GWASCAT Variation in the glucose transporter gene SLC2A2 is associated with glycemic response to metformin. 27500523 2016
dbSNP: rs11924032
rs11924032
Entrez Id: 6514
Gene Symbol: SLC2A2
SLC2A2
CUI: C1305855
Disease:
Body mass index 		A 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs61791109
rs61791109
Entrez Id: 6514
Gene Symbol: SLC2A2
SLC2A2
CUI: C1305855
Disease:
Body mass index 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs7356034
rs7356034
Entrez Id: 6514
Gene Symbol: SLC2A2
SLC2A2
CUI: C1305855
Disease:
Body mass index 		A 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs11720145
rs11720145
Entrez Id: 6514
Gene Symbol: SLC2A2
SLC2A2
CUI: C0202236
Disease:
Triglycerides measurement 		A 0.700 GeneticVariation GWASCAT Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. 30275531 2018
dbSNP: rs11924032
rs11924032
Entrez Id: 6514
Gene Symbol: SLC2A2
SLC2A2
CUI: C0337438
Disease:
Glucose measurement 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018