Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1800574
rs1800574
HNF1A ; HNF1A-AS1
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.850 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci. 22325160

2012
dbSNP: rs2259816
rs2259816
HNF1A
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.820 GeneticVariation GWASDB Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project. 21347282

2011
dbSNP: rs2259816
rs2259816
HNF1A
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		T 0.820 GeneticVariation GWASDB New susceptibility locus for coronary artery disease on chromosome 3q22.3. 19198612

2009
dbSNP: rs1169288
rs1169288
HNF1A ; HNF1A-AS1
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		C 0.800 GeneticVariation GWASDB Discovery and refinement of loci associated with lipid levels. 24097068

2013
dbSNP: rs1169288
rs1169288
HNF1A ; HNF1A-AS1
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		C 0.800 GeneticVariation GWASDB Discovery and refinement of loci associated with lipid levels. 24097068

2013
dbSNP: rs1169288
rs1169288
HNF1A ; HNF1A-AS1
CUI: C1278049
Disease: Serum gamma-glutamyl transferase measurement
Serum gamma-glutamyl transferase measurement 		G 0.800 GeneticVariation GWASDB Loci affecting gamma-glutamyl transferase in adults and adolescents show age × SNP interaction and cardiometabolic disease associations. 22010049

2012
dbSNP: rs1169288
rs1169288
HNF1A ; HNF1A-AS1
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		C 0.800 GeneticVariation GWASDB Biological, clinical and population relevance of 95 loci for blood lipids. 20686565

2010
dbSNP: rs1169288
rs1169288
HNF1A ; HNF1A-AS1
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		C 0.800 GeneticVariation GWASDB Biological, clinical and population relevance of 95 loci for blood lipids. 20686565

2010
dbSNP: rs1169310
rs1169310
HNF1A ; C12orf43
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		G 0.800 GeneticVariation GWASDB New variants including ARG1 polymorphisms associated with C-reactive protein levels identified by genome-wide association and pathway analysis. 24763700

2014
dbSNP: rs1169310
rs1169310
HNF1A ; C12orf43
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		G 0.800 GeneticVariation GWASDB Are C-reactive protein associated genetic variants associated with serum levels and retinal markers of microvascular pathology in Asian populations from Singapore? 23844046

2013
dbSNP: rs1169310
rs1169310
HNF1A ; C12orf43
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		A 0.800 GeneticVariation GWASDB Polymorphisms of the HNF1A gene encoding hepatocyte nuclear factor-1 alpha are associated with C-reactive protein. 18439552

2008
dbSNP: rs1183910
rs1183910
HNF1A
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		G 0.800 GeneticVariation GWASDB Are C-reactive protein associated genetic variants associated with serum levels and retinal markers of microvascular pathology in Asian populations from Singapore? 23844046

2013
dbSNP: rs1183910
rs1183910
HNF1A
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.800 GeneticVariation GWASDB Genome-wide association with C-reactive protein levels in CLHNS: evidence for the CRP and HNF1A loci and their interaction with exposure to a pathogenic environment. 21647738

2012
dbSNP: rs1183910
rs1183910
HNF1A
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		G 0.800 GeneticVariation GWASDB Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. 21300955

2011
dbSNP: rs1183910
rs1183910
HNF1A
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		T 0.800 GeneticVariation GWASDB Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease. 19567438

2009
dbSNP: rs12427353
rs12427353
HNF1A
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.800 GeneticVariation GWASDB Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes. 22885922

2012
dbSNP: rs2244608
rs2244608
HNF1A ; HNF1A-AS1
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622

2012
dbSNP: rs2259816
rs2259816
HNF1A
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		G 0.800 GeneticVariation GWASDB New variants including ARG1 polymorphisms associated with C-reactive protein levels identified by genome-wide association and pathway analysis. 24763700

2014
dbSNP: rs2259816
rs2259816
HNF1A
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		T 0.800 GeneticVariation GWASDB Are C-reactive protein associated genetic variants associated with serum levels and retinal markers of microvascular pathology in Asian populations from Singapore? 23844046

2013
dbSNP: rs2259816
rs2259816
HNF1A
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		T 0.800 GeneticVariation GWASDB Genome-wide association and population genetic analysis of C-reactive protein in African American and Hispanic American women. 22939635

2012
dbSNP: rs2393791
rs2393791
HNF1A
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		C 0.800 GeneticVariation GWASDB New variants including ARG1 polymorphisms associated with C-reactive protein levels identified by genome-wide association and pathway analysis. 24763700

2014
dbSNP: rs2393791
rs2393791
HNF1A
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		T 0.800 GeneticVariation GWASDB Are C-reactive protein associated genetic variants associated with serum levels and retinal markers of microvascular pathology in Asian populations from Singapore? 23844046

2013
dbSNP: rs7310409
rs7310409
HNF1A
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		A 0.800 GeneticVariation GWASDB New variants including ARG1 polymorphisms associated with C-reactive protein levels identified by genome-wide association and pathway analysis. 24763700

2014
dbSNP: rs7310409
rs7310409
HNF1A
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		G 0.800 GeneticVariation GWASDB Are C-reactive protein associated genetic variants associated with serum levels and retinal markers of microvascular pathology in Asian populations from Singapore? 23844046

2013
dbSNP: rs7310409
rs7310409
HNF1A
CUI: C1278049
Disease: Serum gamma-glutamyl transferase measurement
Serum gamma-glutamyl transferase measurement 		G 0.800 GeneticVariation GWASDB Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma. 22001757

2011