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: chr11:6618915:C>T
 
ClinVar:           chr11:6618915:GC>G 		NM_000391.3(TPP1):c.90del Deletion
Pathogenic Condition: not provided
Neuronal ceroid lipofuscinosis 2		 Criteria Provided
Single Submitter

2 SubmittersRCV003005583RCV005608824