Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7164883
rs7164883
0.820 GeneticVariation BEFREE <b>Conclusion:</b><i>HCN4</i> rs498005 and rs7164883 polymorphisms are significantly associated with AF risk. 31315459

2019

dbSNP: rs7164883
rs7164883
0.820 GeneticVariation BEFREE One interaction, between rs7164883 at the HCN4 locus and rs4980345 at the SLC28A1 locus, was found to be significantly associated with AF in the discovery cohorts (interaction OR = 1.44, 95% CI: 1.27-1.65, P = 4.3 × 10<sup>-8</sup>). 27824142

2016

dbSNP: rs7164883
rs7164883
G 0.820 GeneticVariation GWASCAT Meta-analysis identifies six new susceptibility loci for atrial fibrillation. 22544366

2012

dbSNP: rs7164883
rs7164883
G 0.820 GeneticVariation GWASDB Meta-analysis identifies six new susceptibility loci for atrial fibrillation. 22544366

2012

dbSNP: rs148398509
rs148398509
0.010 GeneticVariation BEFREE In conclusion HCN4-P883R may increase ectopic trigger and maintenance of AF by shifting the activation voltage of I<sub>f</sub> to more positive potentials and producing higher current density. 31481236

2019

dbSNP: rs498005
rs498005
0.010 GeneticVariation BEFREE <b>Conclusion:</b><i>HCN4</i> rs4980</span>05 and rs7164883 polymorphisms are significantly associated with AF risk. 31315459

2019

dbSNP: rs1457768351
rs1457768351
0.010 GeneticVariation BEFREE Our findings are consistent with HCN4 haploinsufficiency as the likely mechanism for early-onset AF in the p.Pro257Ser carrier. 24607718

2014