Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs730880702
rs730880702
MYBPC3
G 0.700 GeneticVariation CLINVAR Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples. 27532257

2017
dbSNP: rs730880702
rs730880702
MYBPC3
G 0.700 GeneticVariation CLINVAR Genetics of hypertrophic cardiomyopathy in Norway. 24111713

2014
dbSNP: rs730880702
rs730880702
MYBPC3
G 0.700 GeneticVariation CLINVAR Long-term outcome of 4 Korean families with hypertrophic cardiomyopathy caused by 4 different mutations. 20641121

2010