Gene: ACE ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1267969615
rs1267969615
ACE
0.020 GeneticVariation BEFREE Also, 235TT genotype of AGT (M235T) was significantly associated with enhanced risk of the disease phenotype in HCM, DCM, and RCM. 28120210

2017
dbSNP: rs1267969615
rs1267969615
ACE
0.020 GeneticVariation BEFREE The AGT M235T polymorphism did not significantly affect the risk of HCM. 24204726

2013
dbSNP: rs371010069
rs371010069
ACE
0.010 GeneticVariation BEFREE Several mutations such as Arg403Gln and Arg719Gln are associated with a high incidence of SCD, while Leu908Val mutation is associated with a benign course and a low incidence of SCD in HCM families. 7788945

1995