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: chr20:62836340:C>CGCTTTTCCG
 
ClinVar:           chr20:62836340:C>T 		NM_001853.4(COL9A3):c.1548+7C>T SNV
Conflicting classifications of pathogenicity Condition: not provided Criteria Provided
Conflicting Classifications

2 SubmittersRCV000595536