ARHGAP42, Rho GTPase activating protein 42, 143872

N. diseases: 25; N. variants: 14
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs633185
rs633185
Entrez Id: 143872
Gene Symbol: ARHGAP42
ARHGAP42
CUI: C0005823
Disease:
Blood Pressure 		0.800 GeneticVariation GWASCAT Genetic overlap of chronic obstructive pulmonary disease and cardiovascular disease-related traits: a large-scale genome-wide cross-trait analysis. 30940143 2019
dbSNP: rs633185
rs633185
Entrez Id: 143872
Gene Symbol: ARHGAP42
ARHGAP42
CUI: C0020538
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
Entrez Id: 143872
Gene Symbol: ARHGAP42
ARHGAP42
CUI: C0020538
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
Entrez Id: 143872
Gene Symbol: ARHGAP42
ARHGAP42
CUI: C0020538
Disease:
Hypertensive disease 		G 0.800 GeneticVariation GWASDB Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. 21909115 2011
dbSNP: rs633185
rs633185
Entrez Id: 143872
Gene Symbol: ARHGAP42
ARHGAP42
CUI: C0005823
Disease:
Blood Pressure 		G 0.800 GeneticVariation GWASDB Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure. 21909110 2011
dbSNP: rs10895025
rs10895025
Entrez Id: 143872
Gene Symbol: ARHGAP42
ARHGAP42
CUI: C0871470
Disease:
Systolic Pressure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs604723
rs604723
Entrez Id: 143872
Gene Symbol: ARHGAP42
ARHGAP42
CUI: C0007222
Disease:
Cardiovascular Diseases 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs604723
rs604723
Entrez Id: 143872
Gene Symbol: ARHGAP42
ARHGAP42
CUI: C0871470
Disease:
Systolic Pressure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs633185
rs633185
Entrez Id: 143872
Gene Symbol: ARHGAP42
ARHGAP42
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease 		0.700 GeneticVariation GWASCAT Genetic overlap of chronic obstructive pulmonary disease and cardiovascular disease-related traits: a large-scale genome-wide cross-trait analysis. 30940143 2019
dbSNP: rs73003836
rs73003836
Entrez Id: 143872
Gene Symbol: ARHGAP42
ARHGAP42
CUI: C0427460
Disease:
Red cell distribution width determination 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs73003836
rs73003836
Entrez Id: 143872
Gene Symbol: ARHGAP42
ARHGAP42
CUI: C1304746
Disease:
RDW - Red blood cell distribution width result 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1502284
rs1502284
Entrez Id: 143872
Gene Symbol: ARHGAP42
ARHGAP42
CUI: C0428886
Disease:
Mean blood pressure 		T 0.700 GeneticVariation GWASCAT Interethnic analyses of blood pressure loci in populations of East Asian and European descent. 30487518 2018
dbSNP: rs1502284
rs1502284
Entrez Id: 143872
Gene Symbol: ARHGAP42
ARHGAP42
CUI: C0428883
Disease:
Diastolic blood pressure 		T 0.700 GeneticVariation GWASCAT Interethnic analyses of blood pressure loci in populations of East Asian and European descent. 30487518 2018
dbSNP: rs17654410
rs17654410
Entrez Id: 143872
Gene Symbol: ARHGAP42
ARHGAP42
CUI: C1837461
Disease:
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs17654410
rs17654410
Entrez Id: 143872
Gene Symbol: ARHGAP42
ARHGAP42
CUI: C0410702
Disease:
Adolescent idiopathic scoliosis 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs4754698
rs4754698
Entrez Id: 143872
Gene Symbol: ARHGAP42
ARHGAP42
CUI: C1956346
Disease:
Coronary Artery Disease 		C 0.700 GeneticVariation GWASCAT Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease. 29212778 2018
dbSNP: rs604723
rs604723
Entrez Id: 143872
Gene Symbol: ARHGAP42
ARHGAP42
CUI: C0428886
Disease:
Mean blood pressure 		T 0.700 GeneticVariation GWASCAT Interethnic analyses of blood pressure loci in populations of East Asian and European descent. 30487518 2018
dbSNP: rs604723
rs604723
Entrez Id: 143872
Gene Symbol: ARHGAP42
ARHGAP42
CUI: C0871470
Disease:
Systolic Pressure 		T 0.700 GeneticVariation GWASCAT Interethnic analyses of blood pressure loci in populations of East Asian and European descent. 30487518 2018
dbSNP: rs604723
rs604723
Entrez Id: 143872
Gene Symbol: ARHGAP42
ARHGAP42
CUI: C1956346
Disease:
Coronary Artery Disease 		T 0.700 GeneticVariation GWASCAT Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease. 29212778 2018
dbSNP: rs604723
rs604723
Entrez Id: 143872
Gene Symbol: ARHGAP42
ARHGAP42
CUI: C0428883
Disease:
Diastolic blood pressure 		T 0.700 GeneticVariation GWASCAT Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries. 29912962 2018
dbSNP: rs604723
rs604723
Entrez Id: 143872
Gene Symbol: ARHGAP42
ARHGAP42
CUI: C0001948
Disease:
Alcohol consumption 		T 0.700 GeneticVariation GWASCAT Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries. 29912962 2018
dbSNP: rs604723
rs604723
Entrez Id: 143872
Gene Symbol: ARHGAP42
ARHGAP42
CUI: C0428886
Disease:
Mean blood pressure 		T 0.700 GeneticVariation GWASCAT Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries. 29912962 2018
dbSNP: rs604723
rs604723
Entrez Id: 143872
Gene Symbol: ARHGAP42
ARHGAP42
CUI: C0428883
Disease:
Diastolic blood pressure 		T 0.700 GeneticVariation GWASCAT Interethnic analyses of blood pressure loci in populations of East Asian and European descent. 30487518 2018
dbSNP: rs604723
rs604723
Entrez Id: 143872
Gene Symbol: ARHGAP42
ARHGAP42
CUI: C0020538
Disease:
Hypertensive disease 		T 0.700 GeneticVariation GWASCAT Interethnic analyses of blood pressure loci in populations of East Asian and European descent. 30487518 2018
dbSNP: rs604723
rs604723
Entrez Id: 143872
Gene Symbol: ARHGAP42
ARHGAP42
CUI: C1305849
Disease:
Diastolic blood pressure measurement 		T 0.700 GeneticVariation GWASCAT Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries. 29912962 2018