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: chr19:35848087:C>T
 
ClinVar:           chr19:35848087:C>T 		NM_004646.4(NPHS1):c.1394G>A (p.Cys465Tyr) SNV
Pathogenic Finnish congenital nephrotic syndrome Criteria Provided
Single Submitter

2 SubmittersRCV000049852