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: chr13:38690828:C>T
 
ClinVar:           chr13:38690828:C>T 		NM_207361.6(FREM2):c.3484C>T (p.Arg1162Ter) SNV
Pathogenic Condition: not provided Criteria Provided
Single Submitter

1 SubmittersRCV003868561