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: chr3:121799204:C>T
 
ClinVar:           chr3:121799204:GC>G 		NM_001023570.4(IQCB1):c.758del (p.Cys253fs) Deletion
Pathogenic Nephronophthisis
Senior-Loken syndrome 5		 Criteria Provided
Single Submitter

2 SubmittersRCV001328085RCV003462849