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: chr2:29071171:T>G
 
ClinVar:           chr2:29071171:T>TG 		NM_001029883.3(PCARE):c.3090dup (p.Ser1031fs) Duplication
Pathogenic Condition: not provided Criteria Provided
Single Submitter

1 SubmittersRCV001873182