Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6584555
rs6584555
NEURL1
0.740 GeneticVariation BEFREE We did not find significant association between SNP rs2595104 and rs6584555 andAF. 31039368

2019
dbSNP: rs6584555
rs6584555
NEURL1
0.740 GeneticVariation BEFREE Significant allelic and genotypic associations were identified between NEURL variant rs6584555 and GJA1 variant rs13216675 and AF. 29459676

2018
dbSNP: rs6584555
rs6584555
NEURL1
0.740 GeneticVariation BEFREE Six single-nucleotide polymorphisms-rs593479 (1q24 in PRRX1), rs1906617 (4q25 near PITX2), rs11773845 (7q31 in CAV1), rs6584555 (10q25 in NEURL), rs6490029 (12q24 in CUX2), and rs12932445 (16q22 in ZFHX3) (P < 1.9 × 10<sup>-5</sup>)-were confirmed as being associated with AF. 28129963

2017
dbSNP: rs6584555
rs6584555
NEURL1
C 0.740 GeneticVariation GWASCAT Korean atrial fibrillation network genome-wide association study for early-onset atrial fibrillation identifies novel susceptibility loci. 28460022

2017
dbSNP: rs6584555
rs6584555
NEURL1
0.740 GeneticVariation BEFREE NEURL rs6584555 and CAND2 rs4642101 contribute to postoperative atrial fibrillation: a prospective study among Chinese population. 27203392

2016