Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2681472
rs2681472
ATP2B1
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		A 0.860 GeneticVariation GWASCAT Interethnic analyses of blood pressure loci in populations of East Asian and European descent. 30487518

2018
dbSNP: rs2681472
rs2681472
ATP2B1
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		A 0.860 GeneticVariation GWASCAT Genome-wide association study of blood pressure and hypertension. 19430479

2009
dbSNP: rs1799945
rs1799945
HFE ; LOC108783645
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		G 0.840 GeneticVariation GWASCAT Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. 21909115

2011
dbSNP: rs13333226
rs13333226
UMOD
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		A 0.810 GeneticVariation GWASCAT Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension. 27618447

2016
dbSNP: rs13333226
rs13333226
UMOD
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		A 0.810 GeneticVariation GWASCAT In a subset of 13,446 individuals with estimated glomerular filtration rate (eGFR) measurements, we show that rs13333226 is independently associated with hypertension (unadjusted for eGFR: 0.89 [0.83-0.96], p = 0.004; after eGFR adjustment: 0.89 [0.83-0.96], p = 0.003). 21082022

2010
dbSNP: rs2932538
rs2932538
MOV10
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		G 0.810 GeneticVariation GWASCAT Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. 21909115

2011
dbSNP: rs4373814
rs4373814
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		G 0.810 GeneticVariation GWASCAT Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. 21909115

2011
dbSNP: rs6596140
rs6596140
FSTL4
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		T 0.810 GeneticVariation GWASCAT Using a family-based association test, we found an association with SNPs on chromosome 5q31.1 (rs6596140; P<9 × 10(-8)) for hypertension. 22384028

2012
dbSNP: rs11014166
rs11014166
CACNB2
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		A 0.800 GeneticVariation GWASCAT Genome-wide association study of blood pressure and hypertension. 19430479

2009
dbSNP: rs1173771
rs1173771
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		G 0.800 GeneticVariation GWASCAT Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. 21909115

2011
dbSNP: rs11953630
rs11953630
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		T 0.800 GeneticVariation GWASCAT Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. 21909115

2011
dbSNP: rs13107325
rs13107325
SLC39A8
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		T 0.800 GeneticVariation GWASCAT Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. 21909115

2011
dbSNP: rs16982520
rs16982520
ZNF831
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		A 0.800 GeneticVariation GWASCAT Genome-wide association study of blood pressure and hypertension. 19430479

2009
dbSNP: rs17249754
rs17249754
ATP2B1
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.800 GeneticVariation GWASCAT Structural equation modeling for hypertension and type 2 diabetes based on multiple SNPs and multiple phenotypes. 31513605

2019
dbSNP: rs17249754
rs17249754
ATP2B1
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		A 0.800 GeneticVariation GWASCAT Interethnic analyses of blood pressure loci in populations of East Asian and European descent. 30487518

2018
dbSNP: rs17249754
rs17249754
ATP2B1
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		G 0.800 GeneticVariation GWASCAT Genome-wide association study in Chinese identifies novel loci for blood pressure and hypertension. 25249183

2015
dbSNP: rs2521501
rs2521501
FES
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		T 0.800 GeneticVariation GWASCAT Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. 21909115

2011
dbSNP: rs2820037
rs2820037
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		T 0.800 GeneticVariation GWASCAT Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. 17554300

2007
dbSNP: rs6015450
rs6015450
ZNF831
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		G 0.800 GeneticVariation GWASCAT Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. 21909115

2011
dbSNP: rs633185
rs633185
ARHGAP42
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		C 0.800 GeneticVariation GWASCAT Interethnic analyses of blood pressure loci in populations of East Asian and European descent. 30487518

2018
dbSNP: rs633185
rs633185
ARHGAP42
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		G 0.800 GeneticVariation GWASCAT Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. 21909115

2011
dbSNP: rs805303
rs805303
BAG6
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		G 0.800 GeneticVariation GWASCAT Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. 21909115

2011
dbSNP: rs932764
rs932764
PLCE1
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		G 0.800 GeneticVariation GWASCAT Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. 21909115

2011
dbSNP: rs11191548
rs11191548
CNNM2
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		T 0.780 GeneticVariation GWASCAT Interethnic analyses of blood pressure loci in populations of East Asian and European descent. 30487518

2018
dbSNP: rs1004467
rs1004467
CYP17A1 ; CYP17A1-AS1
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		A 0.760 GeneticVariation GWASCAT Interethnic analyses of blood pressure loci in populations of East Asian and European descent. 30487518

2018