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: chr10:43100528:C>T
 
ClinVar:           chr10:43100528:C>T 		NM_020975.6(RET):c.143C>T (p.Thr48Met) SNV
Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome
Multiple endocrine neoplasia, type 2
Multiple endocrine neoplasia type 2A
Condition: not provided		 Criteria Provided
Conflicting Classifications

6 SubmittersRCV001011585RCV001069718RCV003447573RCV004783877