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: chr13:110183160:G>C
 
ClinVar:           chr13:110183160:CGGTGAGCTGGAATTCCAATCGTACCTTGGGGACCTGGGAAGCCT>C 		NM_001845.6(COL4A1):c.1971_1990+24del Deletion
Likely pathogenic Condition: not provided Criteria Provided
Single Submitter

1 SubmittersRCV002019950