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: 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
dbSNP: rs13428598
rs13428598
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C0596887
Disease:
mathematical ability 		T 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: 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: C0155922
Disease:
Tooth development and eruption disorder 		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: C0399352
Disease:
Developmental absence of tooth 		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: rs2034604
rs2034604
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C4082304
Disease:
Oligodontia 		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: C4310638
Disease:
TOOTH AGENESIS, SELECTIVE, 9 		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: C1970117
Disease:
Tooth Agenesis, Selective, With Orofacial Cleft 		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: C3489529
Disease:
Tooth Agenesis, Familial 		T 0.700 GeneticVariation GWASCAT Rare and Common Variants Conferring Risk of Tooth Agenesis. 29364747 2018
dbSNP: rs34030812
rs34030812
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C1269683
Disease:
Major Depressive Disorder 		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: rs34030812
rs34030812
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C0525045
Disease:
Mood Disorders 		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: rs35825582
rs35825582
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C0525045
Disease:
Mood Disorders 		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: rs35825582
rs35825582
Entrez Id: 55843
Gene Symbol: ARHGAP15
ARHGAP15
CUI: C1269683
Disease:
Major Depressive Disorder 		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: 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: rs6721148
rs6721148
Entrez Id: 55843;105373654
Gene Symbol: ARHGAP15;ARHGAP15-AS1
ARHGAP15;ARHGAP15-AS1
CUI: C0596887
Disease:
mathematical ability 		T 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: 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: 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: 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: 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: 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