Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1799945
rs1799945
HFE ; LOC108783645
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		G 0.840 GeneticVariation GWASDB Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. 21909115

2011
dbSNP: rs1799945
rs1799945
HFE ; LOC108783645
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.800 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517

2012
dbSNP: rs1799945
rs1799945
HFE ; LOC108783645
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.800 GeneticVariation GWASDB Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levels. 19820698

2009
dbSNP: rs1800562
rs1800562
HFE ; LOC108783645
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		A 0.800 GeneticVariation GWASDB GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children. 23263863

2013
dbSNP: rs1800562
rs1800562
HFE ; LOC108783645
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		A 0.800 GeneticVariation GWASDB Discovery and refinement of loci associated with lipid levels. 24097068

2013
dbSNP: rs1800562
rs1800562
HFE ; LOC108783645
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		A 0.800 GeneticVariation GWASDB Discovery and refinement of loci associated with lipid levels. 24097068

2013
dbSNP: rs1800562
rs1800562
HFE ; LOC108783645
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.800 GeneticVariation GWASDB Genetic Loci implicated in erythroid differentiation and cell cycle regulation are associated with red blood cell traits. 22560525

2012
dbSNP: rs1800562
rs1800562
HFE ; LOC108783645
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.800 GeneticVariation GWASDB Genetic Loci implicated in erythroid differentiation and cell cycle regulation are associated with red blood cell traits. 22560525

2012
dbSNP: rs1800562
rs1800562
HFE ; LOC108783645
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.800 GeneticVariation GWASDB Genetic Loci implicated in erythroid differentiation and cell cycle regulation are associated with red blood cell traits. 22560525

2012
dbSNP: rs1800562
rs1800562
HFE ; LOC108783645
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		A 0.800 GeneticVariation GWASDB Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. 21665994

2011
dbSNP: rs1800562
rs1800562
HFE ; LOC108783645
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		A 0.800 GeneticVariation GWASDB Biological, clinical and population relevance of 95 loci for blood lipids. 20686565

2010
dbSNP: rs1800562
rs1800562
HFE ; LOC108783645
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		A 0.800 GeneticVariation GWASDB Biological, clinical and population relevance of 95 loci for blood lipids. 20686565

2010
dbSNP: rs1800562
rs1800562
HFE ; LOC108783645
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		A 0.800 GeneticVariation GWASDB Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. 19862010

2009
dbSNP: rs1800562
rs1800562
HFE ; LOC108783645
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		A 0.800 GeneticVariation GWASDB Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. 19862010

2009
dbSNP: rs1800562
rs1800562
HFE ; LOC108783645
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		A 0.800 GeneticVariation GWASDB Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. 19862010

2009
dbSNP: rs12346
rs12346
HFE
CUI: C0018099
Disease: Gout
Gout 		0.700 GeneticVariation GWASDB Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. 23263486

2013
dbSNP: rs12346
rs12346
HFE
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty 		0.700 GeneticVariation GWASDB Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. 23263486

2013
dbSNP: rs12346
rs12346
HFE
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517

2012
dbSNP: rs12346
rs12346
HFE
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty 		0.700 GeneticVariation GWASDB Genome-wide association study for serum urate concentrations and gout among African Americans identifies genomic risk loci and a novel URAT1 loss-of-function allele. 21768215

2011
dbSNP: rs12346
rs12346
HFE
CUI: C0018099
Disease: Gout
Gout 		0.700 GeneticVariation GWASDB Genome-wide association study for serum urate concentrations and gout among African Americans identifies genomic risk loci and a novel URAT1 loss-of-function allele. 21768215

2011
dbSNP: rs1572982
rs1572982
HFE
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty 		0.700 GeneticVariation GWASDB Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. 23263486

2013
dbSNP: rs1572982
rs1572982
HFE
CUI: C0018099
Disease: Gout
Gout 		0.700 GeneticVariation GWASDB Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. 23263486

2013
dbSNP: rs1799945
rs1799945
HFE ; LOC108783645
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 GeneticVariation GWASDB Blood pressure loci identified with a gene-centric array. 22100073

2011
dbSNP: rs1799945
rs1799945
HFE ; LOC108783645
CUI: C1305849
Disease: Diastolic blood pressure measurement
Diastolic blood pressure measurement 		G 0.700 GeneticVariation GWASDB Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. 21909115

2011
dbSNP: rs1799945
rs1799945
HFE ; LOC108783645
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 GeneticVariation GWASDB Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure. 21909110

2011