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: chr1:171103822:C>G
 
ClinVar:           chr1:171103822:C>G 		NM_001002294.3(FMO3):c.170C>G (p.Ser57Ter) SNV
Pathogenic Condition: not provided Criteria Provided
Single Submitter

1 SubmittersRCV003562839