Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs13025591
rs13025591
Entrez Id: 116987
Gene Symbol: AGAP1
AGAP1
CUI: C0036341
Disease:
Schizophrenia
0.800 GeneticVariation GWASDB Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder. 22688191 2012
dbSNP: rs13025591
rs13025591
Entrez Id: 116987
Gene Symbol: AGAP1
AGAP1
CUI: C0036341
Disease:
Schizophrenia
0.800 GeneticVariation GWASCAT Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder. 22688191 2012
dbSNP: rs13025591
rs13025591
Entrez Id: 116987
Gene Symbol: AGAP1
AGAP1
CUI: C0036341
Disease:
Schizophrenia
0.800 GeneticVariation GWASDB Common variants on chromosome 6p22.1 are associated with schizophrenia. 19571809 2009
dbSNP: rs10208807
rs10208807
Entrez Id: 116987
Gene Symbol: AGAP1
AGAP1
CUI: C1305855
Disease:
Body mass index
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11676226
rs11676226
Entrez Id: 116987
Gene Symbol: AGAP1
AGAP1
CUI: C0005890
Disease:
Body Height
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs55823170
rs55823170
Entrez Id: 116987
Gene Symbol: AGAP1
AGAP1
CUI: C0042834
Disease:
Vital capacity
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs908443
rs908443
Entrez Id: 116987
Gene Symbol: AGAP1
AGAP1
CUI: C1305855
Disease:
Body mass index
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs9808302
rs9808302
Entrez Id: 116987
Gene Symbol: AGAP1
AGAP1
CUI: C1305855
Disease:
Body mass index
A 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs987071
rs987071
Entrez Id: 116987
Gene Symbol: AGAP1
AGAP1
CUI: C1305855
Disease:
Body mass index
T 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs10190094
rs10190094
Entrez Id: 116987
Gene Symbol: AGAP1
AGAP1
CUI: C0409959
Disease:
Osteoarthritis, Knee
G 0.700 GeneticVariation GWASCAT Genome-wide analyses using UK Biobank data provide insights into the genetic architecture of osteoarthritis. 29559693 2018
dbSNP: rs12471554
rs12471554
Entrez Id: 116987
Gene Symbol: AGAP1
AGAP1
CUI: C0596887
Disease:
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: rs10929159
rs10929159
Entrez Id: 116987
Gene Symbol: AGAP1
AGAP1
CUI: C0030567
Disease:
Parkinson Disease
A 0.700 GeneticVariation GWASCAT A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci. 28892059 2017
dbSNP: rs3754648
rs3754648
Entrez Id: 116987
Gene Symbol: AGAP1
AGAP1
CUI: C0265240
Disease:
Goldenhar Syndrome
G 0.700 GeneticVariation GWASCAT Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia. 26853712 2016
dbSNP: rs3768939
rs3768939
Entrez Id: 116987
Gene Symbol: AGAP1
AGAP1
CUI: C0020538
Disease:
Hypertensive disease
A 0.700 GeneticVariation GWASCAT Drug-Gene Interactions of Antihypertensive Medications and Risk of Incident Cardiovascular Disease: A Pharmacogenomics Study from the CHARGE Consortium. 26516778 2015
dbSNP: rs3768939
rs3768939
Entrez Id: 116987
Gene Symbol: AGAP1
AGAP1
CUI: C0007222
Disease:
Cardiovascular Diseases
A 0.700 GeneticVariation GWASCAT Drug-Gene Interactions of Antihypertensive Medications and Risk of Incident Cardiovascular Disease: A Pharmacogenomics Study from the CHARGE Consortium. 26516778 2015