Indigenome VS ClinVar IDs Relevant information available in ClinVar
Variant Identifiers ClinVar Name Variant Type Clinical Significance Phenotype Condition Review Status Variation/condition record
IndiGenomes: chr19:55156659:T>C
 
ClinVar:           chr19:55156659:T>C 		NM_000363.5(TNNI3):c.109-15A>G SNV
Conflicting classifications of pathogenicity not specified
Dilated cardiomyopathy 2A
Cardiomyopathy
Hypertrophic cardiomyopathy 7
Cardiomyopathy, familial restrictive, 1
Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome
Hypertrophic cardiomyopathy		 Criteria Provided
Conflicting Classifications

5 SubmittersRCV000218638RCV001133668RCV001190732RCV001133667RCV001133665RCV001133666RCV002518212