Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17426174
rs17426174
LINC02210-CRHR1
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: 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: C0037019
Disease: Shy-Drager Syndrome
Shy-Drager Syndrome 		G 0.700 GeneticVariation GWASCAT A genome-wide association study in multiple system atrophy. 27629089

2016
dbSNP: rs9303521
rs9303521
LINC02210-CRHR1
CUI: C0393571
Disease: Multiple System Atrophy
Multiple System Atrophy 		G 0.700 GeneticVariation GWASCAT A genome-wide association study in multiple system atrophy. 27629089

2016
dbSNP: rs1876829
rs1876829
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		C 0.700 GeneticVariation GWASCAT Association of Genetic Variants Related to Gluteofemoral vs Abdominal Fat Distribution With Type 2 Diabetes, Coronary Disease, and Cardiovascular Risk Factors. 30575882

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: 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: 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: rs143699161
rs143699161
LINC02210-CRHR1 ; LOC105371802
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: rs112550936
rs112550936
LINC02210 ; 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: rs17688916
rs17688916
LINC02210-CRHR1
CUI: C0424574
Disease: Duration of sleep
Duration of sleep 		T 0.700 GeneticVariation GWASCAT Genome-wide association study identifies genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates. 30846698

2019
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: 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: rs393152
rs393152
LINC02210 ; LINC02210-CRHR1
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		A 0.810 GeneticVariation GWASCAT Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575

2009
dbSNP: rs12150672
rs12150672
LINC02210-CRHR1
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		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: 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: rs2942168
rs2942168
LINC02210 ; LINC02210-CRHR1
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		G 0.820 GeneticVariation GWASCAT Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. 21292315

2011
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: rs241036
rs241036
LINC02210 ; LINC02210-CRHR1
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
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
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: 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: 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