Normal allele: AA
Genetic risk factor for ischaemic and haemorrhagic stroke.
Polymorphism rs6843082 is related to topics like this:
Research and publications:
20173747 Common variants in KCNN3 are associated with lone atrial fibrillation.
21245058 Genome-wide association studies of atrial fibrillation: past, present, and future.
22326711 There is power in numbers--even/especially in genomic medicine.
26272656 Korean Atrial Fibrillation (AF) Network: Genetic Variants for AF Do Not Predict Ablation Success.
26660272 Gene-guided therapy for catheter-ablation of atrial fibrillation: are we there yet?
27185397 Exhaustive Genome-Wide Search for SNP-SNP Interactions Across 10 Human Diseases.
27796860 Genetic Risk Factors for Ischemic and Hemorrhagic Stroke.
30182779 Genetic susceptibility to cerebrovascular disease: A systematic review.
30808078 A Genetic Risk Score for Atrial Fibrillation Predicts the Response to Catheter Ablation.
33284871 Personalized warfarin treatment based on the PITX2 single nucleotide polymorphism rs6843082.