Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs727504255
rs727504255
TNNT2
T 0.700 GeneticVariation CLINVAR Use of genetics in the clinical evaluation of cardiomyopathy. 19996403

2009
dbSNP: rs727504255
rs727504255
TNNT2
T 0.700 GeneticVariation CLINVAR Prevalence, clinical significance, and natural history of left ventricular apical aneurysms in hypertrophic cardiomyopathy. 18809796

2008