Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397516915
rs397516915
DSP
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs397516915
rs397516915
DSP
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		T 0.700 CausalMutation CLINVAR