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: 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: rs13002158
rs13002158
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C1305855
Disease:
Body mass index 		A 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs62171698
rs62171698
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C1305855
Disease:
Body mass index 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs6710871
rs6710871
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C1305855
Disease:
Body mass index 		A 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs6710871
rs6710871
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C1305855
Disease:
Body mass index 		A 0.700 GeneticVariation GWASCAT A Large Multiethnic Genome-Wide Association Study of Adult Body Mass Index Identifies Novel Loci. 30108127 2018
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: 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: rs78490412
rs78490412
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
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: rs2034604
rs2034604
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C0399352
Disease:
Developmental absence of tooth 		T 0.700 GeneticVariation GWASCAT Rare and Common Variants Conferring Risk of Tooth Agenesis. 29364747 2018
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: rs7606205
rs7606205
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C0428883
Disease:
Diastolic blood pressure 		A 0.700 GeneticVariation GWASCAT Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. 30224653 2018
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: 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: rs6734367
rs6734367
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C4317009
Disease:
Diverticular Diseases 		G 0.700 GeneticVariation GWASCAT Genome-wide association analyses identify 39 new susceptibility loci for diverticular disease. 30177863 2018
dbSNP: rs6734367
rs6734367
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C4317009
Disease:
Diverticular Diseases 		T 0.700 GeneticVariation GWASCAT Genome-wide association analysis of diverticular disease points towards neuromuscular, connective tissue and epithelial pathomechanisms. 30661054 2019
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: 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: 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: rs16858573
rs16858573
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C0013595
Disease:
Eczema 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs79716587
rs79716587
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2034604
rs2034604
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C0020608
Disease:
Hypodontia 		T 0.700 GeneticVariation GWASCAT Rare and Common Variants Conferring Risk of Tooth Agenesis. 29364747 2018
dbSNP: rs2034604
rs2034604
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C1970118
Disease:
Hypodontia Oligodontia with Orofacial Cleft 		T 0.700 GeneticVariation GWASCAT Rare and Common Variants Conferring Risk of Tooth Agenesis. 29364747 2018
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: 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