rs1289010014, TNNT2

N. diseases: 1
Disease: Hypertrophic Cardiomyopathy ×
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
0.010 GeneticVariation BEFREE Interestingly,TPM1c.842T>C mutation was associated with high penetrance and severe HCM phenotype. 31308319 2019