Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4662344
rs4662344
CUI: C4317009
Disease: Diverticular Diseases
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
CUI: C0012813
Disease: Diverticulitis
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: rs10189912
rs10189912
CUI: C0021704
Disease: Intelligence
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
CUI: C0021704
Disease: Intelligence
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
CUI: C0021704
Disease: Intelligence
Intelligence
0.700 GeneticVariation GWASCAT Large-Scale Cognitive GWAS Meta-Analysis Reveals Tissue-Specific Neural Expression and Potential Nootropic Drug Targets. 29186694

2017

dbSNP: rs10200533
rs10200533
CUI: C0021704
Disease: Intelligence
Intelligence
A 0.700 GeneticVariation GWASCAT A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. 29326435

2019

dbSNP: rs10204230
rs10204230
CUI: C0021704
Disease: Intelligence
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: rs12465778
rs12465778
CUI: C0021704
Disease: Intelligence
Intelligence
T 0.700 GeneticVariation GWASCAT A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. 29326435

2019

dbSNP: rs12991555
rs12991555
CUI: C0596887
Disease: mathematical ability
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: rs13002158
rs13002158
CUI: C1305855
Disease: Body mass index
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: rs13010737
rs13010737
CUI: C1956346
Disease: Coronary Artery 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
CUI: C1269683
Disease: Major Depressive Disorder
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
CUI: C0525045
Disease: Mood Disorders
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
CUI: C0021704
Disease: Intelligence
Intelligence
T 0.700 GeneticVariation GWASCAT Biological annotation of genetic loci associated with intelligence in a meta-analysis of 87,740 individuals. 29520040

2019

dbSNP: rs13428598
rs13428598
CUI: C0021704
Disease: Intelligence
Intelligence
T 0.700 GeneticVariation GWASCAT A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. 29326435

2019

dbSNP: rs13428598
rs13428598
CUI: C0021704
Disease: Intelligence
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
CUI: C0596887
Disease: mathematical ability
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: rs140397066
rs140397066
CUI: C0200635
Disease: Lymphocyte Count measurement
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: rs141234028
rs141234028
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019

dbSNP: rs16858573
rs16858573
CUI: C0013595
Disease: Eczema
Eczema
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019

dbSNP: rs2034604
rs2034604
CUI: C0020608
Disease: Hypodontia
Hypodontia
T 0.700 GeneticVariation GWASCAT Rare and Common Variants Conferring Risk of Tooth Agenesis. 29364747

2018

dbSNP: rs2034604
rs2034604
CUI: C0399352
Disease: Developmental absence of tooth
Developmental absence of tooth
T 0.700 GeneticVariation GWASCAT Rare and Common Variants Conferring Risk of Tooth Agenesis. 29364747

2018

dbSNP: rs2034604
rs2034604
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
CUI: C3489529
Disease: Tooth Agenesis, Familial
Tooth Agenesis, Familial
T 0.700 GeneticVariation GWASCAT Rare and Common Variants Conferring Risk of Tooth Agenesis. 29364747

2018

dbSNP: rs2034604
rs2034604
CUI: C4082304
Disease: Oligodontia
Oligodontia
T 0.700 GeneticVariation GWASCAT Rare and Common Variants Conferring Risk of Tooth Agenesis. 29364747

2018