ARHGAP15, Rho GTPase activating protein 15, 55843

N. diseases: 40; N. variants: 32
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10189773
rs10189773
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		0.700 GeneticVariation GWASDB Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. 17463246 2007
dbSNP: rs9917392
rs9917392
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		0.700 GeneticVariation GWASDB Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. 17463246 2007
dbSNP: rs73962318
rs73962318
Entrez Id: 55843;100873244
Gene Symbol: ARHGAP15;MTND4P22
ARHGAP15;MTND4P22
CUI: C0037369
Disease:
Smoking 		0.700 GeneticVariation GWASCAT Mercapturic Acids Derived from the Toxicants Acrolein and Crotonaldehyde in the Urine of Cigarette Smokers from Five Ethnic Groups with Differing Risks for Lung Cancer. 26053186 2015
dbSNP: rs73962318
rs73962318
Entrez Id: 55843;100873244
Gene Symbol: ARHGAP15;MTND4P22
ARHGAP15;MTND4P22
CUI: C1519383
Disease:
Smoking Behaviors 		0.700 GeneticVariation GWASCAT Mercapturic Acids Derived from the Toxicants Acrolein and Crotonaldehyde in the Urine of Cigarette Smokers from Five Ethnic Groups with Differing Risks for Lung Cancer. 26053186 2015
dbSNP: rs140397066
rs140397066
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C0200635
Disease:
Lymphocyte Count measurement 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs35125029
rs35125029
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C0008810
Disease:
Circadian Rhythms 		0.700 GeneticVariation GWASCAT GWAS of 89,283 individuals identifies genetic variants associated with self-reporting of being a morning person. 26835600 2016
dbSNP: rs74847330
rs74847330
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C3828530
Disease:
Platelet Component Distribution Width Measurement 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs74847330
rs74847330
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C0200665
Disease:
Platelet mean volume determination (procedure) 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs79716587
rs79716587
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C0200635
Disease:
Lymphocyte Count measurement 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs79716587
rs79716587
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C0023508
Disease:
White Blood Cell Count procedure 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs4662344
rs4662344
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C4317009
Disease:
Diverticular Diseases 		0.710 GeneticVariation BEFREE In the combined Icelandic and Danish data sets we observe significant association of intronic variants in ARHGAP15 (Rho GTPase-activating protein 15; rs4662344-T: P=1.9 × 10<sup>-18</sup>, odds ratio (OR)=1.23) and COLQ (collagen-like tail subunit of asymmetric acetylcholinesterase; rs7609897-T: P=1.5 × 10<sup>-10</sup>, OR=0.87) with diverticular disease and in FAM155A (family with sequence similarity 155A; rs67153654-A: P=3.0 × 10<sup>-11</sup>, OR=0.82) with diverticulitis. 28585551 2017
dbSNP: rs4662344
rs4662344
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C0012813
Disease:
Diverticulitis 		T 0.710 GeneticVariation GWASCAT In the combined Icelandic and Danish data sets we observe significant association of intronic variants in ARHGAP15 (Rho GTPase-activating protein 15; rs4662344-T: P=1.9 × 10<sup>-18</sup>, odds ratio (OR)=1.23) and COLQ (collagen-like tail subunit of asymmetric acetylcholinesterase; rs7609897-T: P=1.5 × 10<sup>-10</sup>, OR=0.87) with diverticular disease and in FAM155A (family with sequence similarity 155A; rs67153654-A: P=3.0 × 10<sup>-11</sup>, OR=0.82) with diverticulitis. 28585551 2017
dbSNP: rs4662344
rs4662344
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C4317009
Disease:
Diverticular Diseases 		T 0.710 GeneticVariation GWASCAT In the combined Icelandic and Danish data sets we observe significant association of intronic variants in ARHGAP15 (Rho GTPase-activating protein 15; rs4662344-T: P=1.9 × 10<sup>-18</sup>, odds ratio (OR)=1.23) and COLQ (collagen-like tail subunit of asymmetric acetylcholinesterase; rs7609897-T: P=1.5 × 10<sup>-10</sup>, OR=0.87) with diverticular disease and in FAM155A (family with sequence similarity 155A; rs67153654-A: P=3.0 × 10<sup>-11</sup>, OR=0.82) with diverticulitis. 28585551 2017
dbSNP: rs4662344
rs4662344
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C0012813
Disease:
Diverticulitis 		0.710 GeneticVariation BEFREE In the combined Icelandic and Danish data sets we observe significant association of intronic variants in ARHGAP15 (Rho GTPase-activating protein 15; rs4662344-T: P=1.9 × 10<sup>-18</sup>, odds ratio (OR)=1.23) and COLQ (collagen-like tail subunit of asymmetric acetylcholinesterase; rs7609897-T: P=1.5 × 10<sup>-10</sup>, OR=0.87) with diverticular disease and in FAM155A (family with sequence similarity 155A; rs67153654-A: P=3.0 × 10<sup>-11</sup>, OR=0.82) with diverticulitis. 28585551 2017
dbSNP: rs10191758
rs10191758
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C0021704
Disease:
Intelligence 		A 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis of 78,308 individuals identifies new loci and genes influencing human intelligence. 28530673 2017
dbSNP: rs10191758
rs10191758
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C0021704
Disease:
Intelligence 		0.700 GeneticVariation GWASCAT Large-Scale Cognitive GWAS Meta-Analysis Reveals Tissue-Specific Neural Expression and Potential Nootropic Drug Targets. 29186694 2017
dbSNP: rs74847330
rs74847330
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C1527304
Disease:
Allergic Reaction 		A 0.700 GeneticVariation GWASCAT Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology. 29083406 2017
dbSNP: rs4662344
rs4662344
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C1510475
Disease:
Diverticulosis 		0.010 GeneticVariation BEFREE In the combined Icelandic and Danish data sets we observe significant association of intronic variants in ARHGAP15 (Rho GTPase-activating protein 15; rs4662344-T: P=1.9 × 10<sup>-18</sup>, odds ratio (OR)=1.23) and COLQ (collagen-like tail subunit of asymmetric acetylcholinesterase; rs7609897-T: P=1.5 × 10<sup>-10</sup>, OR=0.87) with diverticular disease and in FAM155A (family with sequence similarity 155A; rs67153654-A: P=3.0 × 10<sup>-11</sup>, OR=0.82) with diverticulitis. 28585551 2017
dbSNP: rs10189912
rs10189912
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C0021704
Disease:
Intelligence 		A 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
dbSNP: rs10204230
rs10204230
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C0021704
Disease:
Intelligence 		T 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
dbSNP: rs12991555
rs12991555
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C0596887
Disease:
mathematical ability 		A 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs13010737
rs13010737
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C1956346
Disease:
Coronary Artery Disease 		A 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: rs13413953
rs13413953
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C1269683
Disease:
Major Depressive Disorder 		G 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways. 29942085 2018
dbSNP: rs13413953
rs13413953
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C0525045
Disease:
Mood Disorders 		G 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways. 29942085 2018
dbSNP: rs13428598
rs13428598
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C0021704
Disease:
Intelligence 		T 0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566 2018