rs397516459, TNNT2

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
0.700 GeneticVariation CLINVAR Clinical challenges of genotype positive (+)-phenotype negative (-) family members in hypertrophic cardiomyopathy. 21185001 2011
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
0.700 GeneticVariation CLINVAR Mutations in Troponin that cause HCM, DCM AND RCM: what can we learn about thin filament function? 19914256 2010
Hypertrophic Cardiomyopathy
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
0.700 GeneticVariation CLINVAR Inherited cardiomyopathies as a troponin disease. 15631686 2004