Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587782962
rs587782962
MYH7
T 0.710 GeneticVariation CLINVAR Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples. 27532257

2017
dbSNP: rs587782962
rs587782962
MYH7
0.710 GeneticVariation BEFREE MYH7-R1053Q was the third most common mutation, and should be screened in all new cases of HCM in Finland. 24888384

2014
dbSNP: rs587782962
rs587782962
MYH7
T 0.710 GeneticVariation CLINVAR A new common mutation in the cardiac beta-myosin heavy chain gene in Finnish patients with hypertrophic cardiomyopathy. 24888384

2014
dbSNP: rs587782962
rs587782962
MYH7
T 0.710 GeneticVariation CLINVAR Two novel mutations in the beta-myosin heavy chain gene associated with dilated cardiomyopathy. 15556047

2004
dbSNP: rs587782962
rs587782962
MYH7
T 0.710 CausalMutation CLINVAR Two novel mutations in the beta-myosin heavy chain gene associated with dilated cardiomyopathy. 15556047

2004