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: chr13:48452979:C>T
 
ClinVar:           chr13:48452979:C>T 		NM_000321.3(RB1):c.1696-14C>T SNV
Conflicting classifications of pathogenicity Condition: not provided
Retinoblastoma		 Criteria Provided
Conflicting Classifications

3 SubmittersRCV002226075RCV003093889