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: chr4:105236588:C>A
 
ClinVar:           chr4:105236588:C>A 		NM_001127208.3(TET2):c.2646C>A (p.Cys882Ter) SNV
Pathogenic Condition: not provided Criteria Provided
Single Submitter

1 SubmittersRCV005203649
IndiGenomes: chr4:105272735:C>T
 
ClinVar:           chr4:105272735:C>T 		NM_001127208.3(TET2):c.4354C>T (p.Arg1452Ter) SNV
Conflicting classifications of pathogenicity Condition: not provided Criteria Provided
Conflicting Classifications

2 SubmittersRCV001768250