Normal allele: CC
Polymorphism rs7193343 is related to topics like this:
Research and publications:
19597491 A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.
20850564 R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation.
21058051 New information on the genetics of stroke.
21245058 Genome-wide association studies of atrial fibrillation: past, present, and future.
21629240 Genetic susceptibility to ischemic stroke.
25684755 Common genetic variants and response to atrial fibrillation ablation.
26660272 Gene-guided therapy for catheter-ablation of atrial fibrillation: are we there yet?
29624624 Genetic modulation of atrial fibrillation risk in a Hispanic/Latino cohort.
30448967 Genotype-phenotype associations in atrial fibrillation: meta-analysis.