Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10824026
rs10824026
SYNPO2L ; LOC105378360
A 0.810 GeneticVariation GWASCAT Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. 28416818

2017
dbSNP: rs10824026
rs10824026
SYNPO2L ; LOC105378360
0.810 GeneticVariation BEFREE The rs10824026 SNP on chromosome 10q22 mediates a modest proportion of the increased risk of AF among white individuals compared with black individuals, potentially through an effect on gene expression levels of MYOZ1. 27438321

2016
dbSNP: rs10824026
rs10824026
SYNPO2L ; LOC105378360
A 0.810 GeneticVariation GWASDB Meta-analysis identifies six new susceptibility loci for atrial fibrillation. 22544366

2012
dbSNP: rs10824026
rs10824026
SYNPO2L ; LOC105378360
A 0.810 GeneticVariation GWASCAT Meta-analysis identifies six new susceptibility loci for atrial fibrillation. 22544366

2012