Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs516514
rs516514
FHOD3
0.710 GeneticVariation GWASDB Formin homology 2 domain containing 3 variants associated with hypertrophic cardiomyopathy. 23255317

2013
dbSNP: rs516514
rs516514
FHOD3
0.710 GeneticVariation BEFREE We identified an intronic FHOD3 variant (rs516514) associated with HCM (odds ratio, 2.45; 95% confidence interval, 1.76-3.41; P=1.25×10(-7)) and validated this finding in an independent cohort. 23255317

2013