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: chr15:68208278:G>C
 
ClinVar:           chr15:68208278:G>A 		NM_017882.3(CLN6):c.798C>T (p.Phe266=) SNV
Conflicting classifications of pathogenicity Condition: not provided
Neuronal ceroid lipofuscinosis		 Criteria Provided
Conflicting Classifications

2 SubmittersRCV000730801RCV001082640