Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12341266
rs12341266
Entrez Id: 5998
Gene Symbol: RGS3
RGS3
CUI: C0007194
Disease:
Hypertrophic Cardiomyopathy
0.700 GeneticVariation GWASDB Formin homology 2 domain containing 3 variants associated with hypertrophic cardiomyopathy. 23255317 2013