Variant Identifiers	ClinVar Name	Variant Type	Clinical Significance	Phenotype Condition	Review Status	Variation/condition record
Indigenome VS ClinVar IDs	Relevant information available in ClinVar
IndiGenomes: chr10:102593663:C>T ClinVar: chr10:102593663:C>T	NM_016169.4(SUFU):c.625C>T (p.His209Tyr)	SNV	Conflicting classifications of pathogenicity	Gorlin syndrome Medulloblastoma Hereditary cancer-predisposing syndrome	Criteria Provided Conflicting Classifications	3 SubmittersRCV001238659 RCV002256717