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: chr12:68731651:C>T
 
ClinVar:           chr12:68731651:C>T 		NM_020401.4(NUP107):c.1930C>T (p.Arg644Ter) SNV
Pathogenic Condition: not provided Criteria Provided
Single Submitter

1 SubmittersRCV003031434