COL21A1, collagen type XXI alpha 1 chain, 81578

N. diseases: 12; N. variants: 7
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0009171
Disease: Cocaine Abuse
Cocaine Abuse
0.300 Biomarker disease CTD_human Substance dependence low-density whole genome association study in two distinct American populations. 18438686 2008
CUI: C0236736
Disease: Cocaine-Related Disorders
Cocaine-Related Disorders
0.300 Biomarker group CTD_human Substance dependence low-density whole genome association study in two distinct American populations. 18438686 2008
CUI: C0600427
Disease: Cocaine Dependence
Cocaine Dependence
0.300 Biomarker disease CTD_human Substance dependence low-density whole genome association study in two distinct American populations. 18438686 2008
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.100 GeneticVariation phenotype GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.100 GeneticVariation phenotype GWASCAT Trans-ethnic association study of blood pressure determinants in over 750,000 individuals. 30578418 2019
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.100 GeneticVariation phenotype GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.100 GeneticVariation phenotype GWASCAT Trans-ethnic association study of blood pressure determinants in over 750,000 individuals. 30578418 2019
Other and unspecified reactive psychosis
0.100 GeneticVariation disease GWASCAT Genome-wide association study of atypical psychosis. 24132900 2013
CUI: C0033975
Disease: Psychotic Disorders
Psychotic Disorders
0.100 GeneticVariation group GWASCAT Genome-wide association study of atypical psychosis. 24132900 2013
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.100 GeneticVariation phenotype GWASDB Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure. 21909110 2011
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip
0.010 GeneticVariation disease BEFREE Two novel genes TOX3 and COL21A1 in large extended Malay families with nonsyndromic cleft lip and/or palate. 30924295 2019
CUI: C4321245
Disease: Cleft lip or lips
Cleft lip or lips
0.010 GeneticVariation phenotype BEFREE Two novel genes TOX3 and COL21A1 in large extended Malay families with nonsyndromic cleft lip and/or palate. 30924295 2019
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.010 GeneticVariation group BEFREE We identified 30 new blood pressure- or hypertension-associated genetic regions in the general population, including 3 rare missense variants in RBM47, COL21A1 and RRAS with larger effects (>1.5 mm Hg/allele) than common variants. 27618447 2016