Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs148395034
rs148395034
Entrez Id: 84676
Gene Symbol: TRIM63
TRIM63
CUI: C4551472
Disease:
Hypertrophic obstructive cardiomyopathy
0.010 GeneticVariation BEFREE The p.Q247X variant in TRIM63 is not likely to be a highly penetrant variant causing hypertrophic cardiomyopathy. 24436435 2014