Gene: MYOZ1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 58529
Gene Symbol: MYOZ1
MYOZ1 		0.330 Biomarker disease CTD_human Biobank-driven genomic discovery yields new insight into atrial fibrillation biology. 30061737 2018
Entrez Id: 58529
Gene Symbol: MYOZ1
MYOZ1 		0.330 GeneticVariation disease BEFREE The rs10824026 SNP on chromosome 10q22 mediates a modest proportion of the increased risk of AF among white individuals compared with black individuals, potentially through an effect on gene expression levels of MYOZ1. 27438321 2016
Entrez Id: 58529
Gene Symbol: MYOZ1
MYOZ1 		0.330 GeneticVariation disease BEFREE We also confirmed a previously described association between AF risk variants and MYOZ1 expression. 26073630 2015
Entrez Id: 58529
Gene Symbol: MYOZ1
MYOZ1 		0.330 GeneticVariation disease BEFREE Our results implicate MYOZ1 as the causative gene at the chromosome 10q22 locus for AF. 24177373 2014