AOPEP, aminopeptidase O (putative), 84909

N. diseases: 23; N. variants: 58
Disease: Atrial Fibrillation ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10821415
rs10821415
Entrez Id: 84909
Gene Symbol: AOPEP
AOPEP
CUI: C0004238
Disease:
Atrial Fibrillation 		A 0.810 GeneticVariation GWASCAT Biobank-driven genomic discovery yields new insight into atrial fibrillation biology. 30061737 2018
dbSNP: rs10821415
rs10821415
Entrez Id: 84909
Gene Symbol: AOPEP
AOPEP
CUI: C0004238
Disease:
Atrial Fibrillation 		0.810 GeneticVariation BEFREE Three known AF-genetic variants (rs6666258, rs6817105, and rs10821415) were associated with self-terminating AF. 28175276 2017
dbSNP: rs10821415
rs10821415
Entrez Id: 84909
Gene Symbol: AOPEP
AOPEP
CUI: C0004238
Disease:
Atrial Fibrillation 		A 0.810 GeneticVariation GWASCAT Meta-analysis identifies six new susceptibility loci for atrial fibrillation. 22544366 2012
dbSNP: rs10821415
rs10821415
Entrez Id: 84909
Gene Symbol: AOPEP
AOPEP
CUI: C0004238
Disease:
Atrial Fibrillation 		A 0.810 GeneticVariation GWASDB Meta-analysis identifies six new susceptibility loci for atrial fibrillation. 22544366 2012
dbSNP: rs4385527
rs4385527
Entrez Id: 84909
Gene Symbol: AOPEP
AOPEP
CUI: C0004238
Disease:
Atrial Fibrillation 		A 0.700 GeneticVariation GWASCAT Multi-ethnic genome-wide association study for atrial fibrillation. 29892015 2018
dbSNP: rs7026071
rs7026071
Entrez Id: 84909
Gene Symbol: AOPEP
AOPEP
CUI: C0004238
Disease:
Atrial Fibrillation 		T 0.700 GeneticVariation GWASCAT Multi-ethnic genome-wide association study for atrial fibrillation. 29892015 2018
dbSNP: rs7026071
rs7026071
Entrez Id: 84909
Gene Symbol: AOPEP
AOPEP
CUI: C0004238
Disease:
Atrial Fibrillation 		T 0.700 GeneticVariation GWASCAT Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. 28416818 2017