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: chr11:61951945:C>CA
 
ClinVar:           chr11:61951945:C>T 		NM_004183.4(BEST1):c.139C>T (p.Arg47Cys) SNV
Pathogenic/Likely pathogenic Condition: not provided Criteria Provided
Multiple Submitters
No Conflicts

2 SubmittersRCV001376914