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: chr8:54626153:C>T
 
ClinVar:           chr8:54626153:TC>T 		NM_006269.2(RP1):c.2272del (p.His758fs) Deletion
Pathogenic Condition: not provided Criteria Provided
Single Submitter

1 SubmittersRCV002014727