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: chr3:170998308:C>A
 
ClinVar:           chr3:170998308:C>T 		NM_000340.2(SLC2A2):c.1259G>A (p.Trp420Ter) SNV
Pathogenic Fanconi-Bickel syndrome No Assertion Criteria Provided

1 SubmittersRCV000017476