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: chr14:22773652:A>G
 
ClinVar:           chr14:22773652:A>G 		NM_003982.4(SLC7A7):c.1494T>C (p.Asp498=) SNV
Conflicting classifications of pathogenicity Lysinuric protein intolerance Criteria Provided
Conflicting Classifications

4 SubmittersRCV000278758