AGT228912417rs699A or G AA
We observed significant association between tagging-SNP rs699 (M235T), located in exon 2 of the AGT gene, and AF. The AA genotype of rs699 increased the risk of AF by 70% (95% confidence interval, 1.01-2.85; P = .044) under a recessive model (AA vs AG + GG). http://www.sciencedirect.com/science/article/pii/S0022073609005378
ZFHX371586661rs7193343C or T CC
P = 1.4x10-10
A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke-A variant in the ZFHX3 gene on chromosome 16q22, rs7193343-T, associated significantly with AF (odds ratio OR = 1.21, P = 1.4 10-10).
A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke http://www.nature.com/ng/journal/v41/n8/full/ng.417.html
Atrial Natriuretic Peptide Frameshift Mutation in Familial Atrial Fibrillation http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2518320/
For genotype-phenotype association analyses, we assumed an additive-allele model of inheritance and we conducted association tests using regression models with generalized estimating equations (GEE), as well as family-based association testing using FBAT. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1995607/