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: C1306620
Disease: Systolic blood pressure measurement
Systolic 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: C0337439
Disease: Iron measurement
Iron measurement 		C 0.700 GeneticVariation GWASDB Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels. 21208937

2011
dbSNP: rs1799945
rs1799945
HFE ; LOC108783645
CUI: C0428578
Disease: Iron level result
Iron level result 		C 0.700 GeneticVariation GWASDB Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels. 21208937

2011
dbSNP: rs1799945
rs1799945
HFE ; LOC108783645
CUI: C2239101
Disease: Hemoglobin, CTCAE
Hemoglobin, CTCAE 		0.700 GeneticVariation GWASDB Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levels. 19820698

2009
dbSNP: rs1799945
rs1799945
HFE ; LOC108783645
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASDB Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. 19862010

2009
dbSNP: rs1800562
rs1800562
HFE ; LOC108783645
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		A 0.700 GeneticVariation GWASDB Discovery and refinement of loci associated with lipid levels. 24097068

2013
dbSNP: rs1800562
rs1800562
HFE ; LOC108783645
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: rs1800562
rs1800562
HFE ; LOC108783645
CUI: C2239101
Disease: Hemoglobin, CTCAE
Hemoglobin, CTCAE 		0.700 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: C0474535
Disease: Mean corpuscular hemoglobin concentration determination
Mean corpuscular hemoglobin concentration determination 		0.700 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: C1306620
Disease: Systolic blood pressure measurement
Systolic blood pressure measurement 		0.700 GeneticVariation GWASDB Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. 21909115

2011
dbSNP: rs1800562
rs1800562
HFE ; LOC108783645
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement 		A 0.700 GeneticVariation GWASDB Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits. 21943158

2011
dbSNP: rs1800562
rs1800562
HFE ; LOC108783645
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		A 0.700 GeneticVariation GWASDB A genome-wide association study of red blood cell traits using the electronic medical record. 20927387

2010
dbSNP: rs1800562
rs1800562
HFE ; LOC108783645
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		A 0.700 GeneticVariation GWASDB Biological, clinical and population relevance of 95 loci for blood lipids. 20686565

2010
dbSNP: rs1800562
rs1800562
HFE ; LOC108783645
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		A 0.700 GeneticVariation GWASDB A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. 19820697

2009
dbSNP: rs1800562
rs1800562
HFE ; LOC108783645
CUI: C2239101
Disease: Hemoglobin, CTCAE
Hemoglobin, CTCAE 		A 0.700 GeneticVariation GWASDB Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. 19862010

2009
dbSNP: rs1800702
rs1800702
HFE ; LOC108783645
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: rs1800702
rs1800702
HFE ; LOC108783645
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: rs1800702
rs1800702
HFE ; LOC108783645
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: rs1800702
rs1800702
HFE ; LOC108783645
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASDB Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. 19862010

2009
dbSNP: rs2006736
rs2006736
HFE ; LOC108783645
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: rs2006736
rs2006736
HFE ; LOC108783645
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: rs2006736
rs2006736
HFE ; LOC108783645
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: rs2006736
rs2006736
HFE ; LOC108783645
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASDB Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. 19862010

2009
dbSNP: rs2071303
rs2071303
HFE ; LOC108783645
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: rs2071303
rs2071303
HFE ; LOC108783645
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