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: chr1:85267841:G>A
 
ClinVar:           chr1:85267841:G>A 		NM_003921.5(BCL10):c.488C>T (p.Thr163Met) SNV
Pathogenic Malignant tumor of testis No Assertion Criteria Provided

1 SubmittersRCV000023309