Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1289010014
rs1289010014
TNNT2
0.010 GeneticVariation BEFREE Interestingly,TPM1c.842T>C mutation was associated with high penetrance and severe HCM phenotype. 31308319

2019