Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913634
rs121913634
MYH7
0.710 GeneticVariation BEFREE The Arg870His and Asp778Val amino acid alterations were found in 2 unrelated patients with a severe form of hypertrophic cardiomyopathy. 21674835

2011
dbSNP: rs121913634
rs121913634
MYH7
A 0.710 CausalMutation CLINVAR