Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4908760
rs4908760
CUI: C0042900
Disease: Vitiligo
Vitiligo
G 0.800 GeneticVariation GWASCAT Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo. 20410501

2010

dbSNP: rs2252865
rs2252865
Attention deficit hyperactivity disorder
T 0.800 GeneticVariation GWASCAT Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885

2013

dbSNP: rs2252865
rs2252865
Child Development Disorders, Pervasive
T 0.700 GeneticVariation GWASCAT Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885

2013

dbSNP: rs2252865
rs2252865
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
T 0.700 GeneticVariation GWASCAT Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885

2013

dbSNP: rs2252865
rs2252865
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
T 0.700 GeneticVariation GWASCAT Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885

2013

dbSNP: rs2252865
rs2252865
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
T 0.700 GeneticVariation GWASCAT Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885

2013

dbSNP: rs301797
rs301797
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
A 0.700 GeneticVariation GWASCAT Genome-wide association study of schizophrenia in Ashkenazi Jews. 26198764

2015

dbSNP: rs4908769
rs4908769
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965

2016

dbSNP: rs301806
rs301806
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
T 0.700 GeneticVariation GWASCAT Identification of 15 genetic loci associated with risk of major depression in individuals of European descent. 27479909

2016

dbSNP: rs301807
rs301807
CUI: C0042900
Disease: Vitiligo
Vitiligo
A 0.700 GeneticVariation GWASCAT Genome-wide association studies of autoimmune vitiligo identify 23 new risk loci and highlight key pathways and regulatory variants. 27723757

2016

dbSNP: rs34976449
rs34976449
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
TG 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016

dbSNP: rs301807
rs301807
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test)
G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016

dbSNP: rs301807
rs301807
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016

dbSNP: rs159963
rs159963
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil 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: rs142472947
rs142472947
CUI: C0023508
Disease: White Blood Cell Count procedure
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: rs301798
rs301798
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.700 GeneticVariation GWASCAT Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. 28540026

2017

dbSNP: rs301798
rs301798
Child Development Disorders, Pervasive
0.700 GeneticVariation GWASCAT Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. 28540026

2017

dbSNP: rs172531
rs172531
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
G 0.700 GeneticVariation GWASCAT Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia. 28991256

2017

dbSNP: rs301806
rs301806
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
T 0.700 GeneticVariation GWASCAT Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology. 29083406

2017

dbSNP: rs2252865
rs2252865
CUI: C0005938
Disease: Bone Density
Bone Density
T 0.700 GeneticVariation GWASCAT Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects. 29304378

2018

dbSNP: rs34269918
rs34269918
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.700 GeneticVariation GWASCAT Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. 29483656

2018

dbSNP: rs159963
rs159963
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
C 0.700 GeneticVariation GWASCAT Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. 29700475

2018

dbSNP: rs301805
rs301805
CUI: C0004096
Disease: Asthma
Asthma
0.700 GeneticVariation GWASCAT A genome-wide cross-trait analysis from UK Biobank highlights the shared genetic architecture of asthma and allergic diseases. 29785011

2018

dbSNP: rs301805
rs301805
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.700 GeneticVariation GWASCAT A genome-wide cross-trait analysis from UK Biobank highlights the shared genetic architecture of asthma and allergic diseases. 29785011

2018

dbSNP: rs6695867
rs6695867
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
A 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