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: chr11:1763823:G>A
 
ClinVar:           chr11:1763823:G>A 		NM_001909.5(CTSD):c.37C>T (p.Leu13=) SNV
Conflicting classifications of pathogenicity Inborn genetic diseases
Condition: not provided
Neuronal ceroid lipofuscinosis		 Criteria Provided
Conflicting Classifications

3 SubmittersRCV002316092RCV003236838RCV003532251