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: chr11:102083171:A>G
 
ClinVar:           chr11:102083171:A>G 		NM_032930.3(CFAP300):c.776A>G (p.His259Arg) SNV
Pathogenic Ciliary dyskinesia, primary, 38 No Assertion Criteria Provided

1 SubmittersRCV000664433