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: chr3:39391572:T>TG
 
ClinVar:           chr3:39391572:T>TG 		NM_017875.4(SLC25A38):c.409dup (p.Ala137fs) Duplication
Pathogenic Sideroblastic anemia 2
Condition: not provided		 Criteria Provided
Multiple Submitters
No Conflicts

2 SubmittersRCV001526383RCV002568127