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: chr1:99861524:T>G
 
ClinVar:           chr1:99861524:T>G 		NM_000642.3(AGL):c.104T>G (p.Leu35Ter) SNV
Pathogenic Glycogen storage disease type III Criteria Provided
Multiple Submitters
No Conflicts

6 SubmittersRCV000410214