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: chr13:100089159:T>A
 
ClinVar:           chr13:100089159:CT>C 		NM_000282.4(PCCA):c.39del (p.Ala14fs) Deletion
Pathogenic/Likely pathogenic Propionic acidemia Criteria Provided
Multiple Submitters
No Conflicts

2 SubmittersRCV001004385
IndiGenomes: chr13:100268784:G>A
 
ClinVar:           chr13:100268784:G>A 		NM_000282.4(PCCA):c.914+1G>A SNV
Likely pathogenic Propionic acidemia Criteria Provided
Multiple Submitters
No Conflicts

2 SubmittersRCV003009355