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: chr12:110614207:C>CTCCT
 
ClinVar:           chr12:110614207:C>CTCCT 		NM_001082538.3(TCTN1):c.26_29dup (p.Val11fs) Duplication
Pathogenic Joubert syndrome 13 Criteria Provided
Single Submitter

1 SubmittersRCV001335645