Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs35076622
rs35076622
LINC02210-CRHR1
CUI: C0021704
Disease: Intelligence
Intelligence 		A 0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566

2018
dbSNP: rs35116560
rs35116560
LINC02210-CRHR1
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: rs35909029
rs35909029
LINC02210-CRHR1
CUI: C0525045
Disease: Mood Disorders
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: rs35909029
rs35909029
LINC02210-CRHR1
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
dbSNP: rs365825
rs365825
LINC02210 ; LINC02210-CRHR1
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965

2016
dbSNP: rs3843738
rs3843738
LINC02210-CRHR1 ; LOC105371802
CUI: C0021704
Disease: Intelligence
Intelligence 		A 0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566

2018
dbSNP: rs393152
rs393152
LINC02210 ; LINC02210-CRHR1
CUI: C0393570
Disease: Corticobasal degeneration
Corticobasal degeneration 		0.700 GeneticVariation GWASCAT Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy. 26077951

2015
dbSNP: rs4327090
rs4327090
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
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: rs55657917
rs55657917
LINC02210-CRHR1
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		T 0.700 GeneticVariation GWASCAT Genome-wide association study of habitual physical activity in over 377,000 UK Biobank participants identifies multiple variants including CADM2 and APOE. 29899525

2018
dbSNP: rs55657917
rs55657917
LINC02210-CRHR1
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		T 0.700 GeneticVariation GWASCAT GWAS identifies 14 loci for device-measured physical activity and sleep duration. 30531941

2018
dbSNP: rs62057061
rs62057061
LINC02210-CRHR1
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: rs62057061
rs62057061
LINC02210-CRHR1
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: rs62057107
rs62057107
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
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: rs675600
rs675600
LINC02210 ; LINC02210-CRHR1
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
dbSNP: rs675600
rs675600
LINC02210 ; LINC02210-CRHR1
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
dbSNP: rs675600
rs675600
LINC02210 ; LINC02210-CRHR1
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
dbSNP: rs675600
rs675600
LINC02210 ; LINC02210-CRHR1
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
dbSNP: rs7207400
rs7207400
LINC02210-CRHR1
CUI: C0005890
Disease: Body Height
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
dbSNP: rs7207400
rs7207400
LINC02210-CRHR1
CUI: C0003467
Disease: Anxiety
Anxiety 		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: rs7220839
rs7220839
LINC02210-CRHR1
CUI: C0003467
Disease: Anxiety
Anxiety 		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: rs7225384
rs7225384
LINC02210-CRHR1 ; LOC107985028
CUI: C0525045
Disease: Mood Disorders
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: rs7225384
rs7225384
LINC02210-CRHR1 ; LOC107985028
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
dbSNP: rs77804065
rs77804065
LINC02210-CRHR1 ; LOC107985028
CUI: C0018681
Disease: Headache
Headache 		T 0.700 GeneticVariation GWASCAT A Genome-Wide Association Study Finds Genetic Associations with Broadly-Defined Headache in UK Biobank (N=223,773). 29397368

2018
dbSNP: rs9303521
rs9303521
LINC02210-CRHR1
CUI: C0525045
Disease: Mood Disorders
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: rs9303521
rs9303521
LINC02210-CRHR1
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