rs6843082, None

N. diseases: 3
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
0.810 GeneticVariation GWASCAT Multi-ethnic genome-wide association study for atrial fibrillation. 29892015 2018
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
0.810 GeneticVariation GWASCAT Identification of six new genetic loci associated with atrial fibrillation in the Japanese population. 28416822 2017
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
0.810 GeneticVariation GWASCAT Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. 28416818 2017
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
0.810 GeneticVariation BEFREE The SNPs at the PITX2 and ZFHX3 loci, but not the KCNN3 locus, were significantly associated with AF (PITX2/rs6843082_G: odds ratio 3.41, 95% CI 2.55 to 4.55, P=1.32×10(-16); PITX2/rs2200733_T: odds ratio 2.05, 95% CI 1.66 to 2.53, P=2.20×10(-11); ZFHX3/rs2106261_A: odds ratio 2.33, 95% CI 1.87 to 2.91, P=3.75×10(-14); KCNN3/rs13376333_T: odds ratio 1.74, 95% CI 0.93 to 3.25, P=0.085). 26272656 2015
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
0.810 GeneticVariation GWASCAT Common variants in KCNN3 are associated with lone atrial fibrillation. 20173747 2010
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
0.810 GeneticVariation GWASDB Common variants in KCNN3 are associated with lone atrial fibrillation. 20173747 2010
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
0.800 GeneticVariation GWASDB Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies. 23041239 2012
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
0.800 GeneticVariation GWASCAT Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies. 23041239 2012
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
0.010 GeneticVariation BEFREE Our results show that the SNP rs2200733 and rs6843082</span> have </span>no significant associations with IS in additive, dominant, recessive, and allelic models (all p > 0.050). 25711478 2015