Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397516355
rs397516355
Entrez Id: 7137
Gene Symbol: TNNI3
TNNI3
CUI: C0007193
Disease:
Cardiomyopathy, Dilated
T 0.700 CausalMutation CLINVAR Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples. 27532257 2017
dbSNP: rs397516355
rs397516355
Entrez Id: 7137
Gene Symbol: TNNI3
TNNI3
CUI: C0007193
Disease:
Cardiomyopathy, Dilated
T 0.700 CausalMutation CLINVAR The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencing. 24503780 2014
dbSNP: rs397516355
rs397516355
Entrez Id: 7137
Gene Symbol: TNNI3
TNNI3
CUI: C0007193
Disease:
Cardiomyopathy, Dilated
T 0.700 CausalMutation CLINVAR Genetic testing for dilated cardiomyopathy in clinical practice. 22464770 2012
dbSNP: rs397516355
rs397516355
Entrez Id: 7137
Gene Symbol: TNNI3
TNNI3
CUI: C0007193
Disease:
Cardiomyopathy, Dilated
T 0.700 GeneticVariation CLINVAR