Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7653834
rs7653834
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
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: rs1372072
rs1372072
CUI: C0023892
Disease: Biliary cirrhosis
Biliary cirrhosis
A 0.700 GeneticVariation GWASCAT Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. 21399635

2011

dbSNP: rs7613595
rs7613595
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test)
C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016

dbSNP: rs75885714
rs75885714
Chemokine (C-C Motif) Ligand 19 Measurement
C 0.700 GeneticVariation GWASCAT Cross-genetic determination of maternal and neonatal immune mediators during pregnancy. 30134952

2018

dbSNP: rs9852648
rs9852648
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019

dbSNP: rs7613595
rs7613595
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016

dbSNP: rs9821630
rs9821630
Finding of Mean Corpuscular Hemoglobin
G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016

dbSNP: rs73146904
rs73146904
Finding of Mean Corpuscular Hemoglobin
A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016

dbSNP: rs2060597
rs2060597
Finding of Mean Corpuscular Hemoglobin
T 0.700 GeneticVariation GWASCAT Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis. 28017375

2017

dbSNP: rs143759545
rs143759545
Finding of Mean Corpuscular Hemoglobin
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019

dbSNP: rs116577908
rs116577908
Finding of Mean Corpuscular Hemoglobin
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019

dbSNP: rs115792481
rs115792481
Finding of Mean Corpuscular Hemoglobin
0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010

2018

dbSNP: rs9846711
rs9846711
CUI: C0021704
Disease: Intelligence
Intelligence
0.700 GeneticVariation GWASCAT Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways. 31374203

2019

dbSNP: rs748832
rs748832
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: rs748832
rs748832
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: rs73139274
rs73139274
CUI: C0021704
Disease: Intelligence
Intelligence
C 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: rs73139272
rs73139272
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: rs73139272
rs73139272
CUI: C0021704
Disease: Intelligence
Intelligence
0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566

2018

dbSNP: rs6779302
rs6779302
CUI: C0021704
Disease: Intelligence
Intelligence
T 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis of 78,308 individuals identifies new loci and genes influencing human intelligence. 28530673

2017

dbSNP: rs75885714
rs75885714
CUI: C2825877
Disease: Interferon Gamma Measurement
Interferon Gamma Measurement
C 0.700 GeneticVariation GWASCAT Cross-genetic determination of maternal and neonatal immune mediators during pregnancy. 30134952

2018

dbSNP: rs75885714
rs75885714
CUI: C3815172
Disease: Interleukin 1 Beta Measurement
Interleukin 1 Beta Measurement
C 0.700 GeneticVariation GWASCAT Cross-genetic determination of maternal and neonatal immune mediators during pregnancy. 30134952

2018

dbSNP: rs75885714
rs75885714
CUI: C2697758
Disease: Interleukin 10 Measurement
Interleukin 10 Measurement
C 0.700 GeneticVariation GWASCAT Cross-genetic determination of maternal and neonatal immune mediators during pregnancy. 30134952

2018

dbSNP: rs75885714
rs75885714
CUI: C2697779
Disease: Interleukin 2 Measurement
Interleukin 2 Measurement
C 0.700 GeneticVariation GWASCAT Cross-genetic determination of maternal and neonatal immune mediators during pregnancy. 30134952

2018

dbSNP: rs9858071
rs9858071
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
C 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: rs6804663
rs6804663
CUI: C1269683
Disease: Major Depressive Disorder
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