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: chr15:89210759:C>T
 
ClinVar:           chr15:89210759:C>T 		NM_000326.5(RLBP1):c.735G>A (p.Trp245Ter) SNV
Pathogenic Condition: not provided Criteria Provided
Single Submitter

1 SubmittersRCV003578696