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: chr10:84208210:C>T
 
ClinVar:           chr10:84208210:C>T 		NM_033100.4(CDHR1):c.1000C>T (p.Gln334Ter) SNV
Pathogenic Condition: not provided Criteria Provided
Single Submitter

1 SubmittersRCV001383463
IndiGenomes: chr10:84211138:AG>A
 
ClinVar:           chr10:84211138:A>AG 		NM_033100.4(CDHR1):c.1463dup (p.Ser489fs) Duplication
Pathogenic Condition: not provided Criteria Provided
Single Submitter

1 SubmittersRCV001381075