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: chr14:91297486:T>C
 
ClinVar:           chr14:91297486:T>C 		NM_001080414.4(CCDC88C):c.3785A>G (p.Asn1262Ser) SNV
Conflicting classifications of pathogenicity Inborn genetic diseases
Condition: not provided		 Criteria Provided
Conflicting Classifications

2 SubmittersRCV002741977RCV002775179
IndiGenomes: chr14:91314114:G>A
 
ClinVar:           chr14:91314114:G>A 		NM_001080414.4(CCDC88C):c.1702C>T (p.Arg568Ter) SNV
Pathogenic Condition: not provided
Spinocerebellar ataxia type 40		 Criteria Provided
Single Submitter

2 SubmittersRCV003721104RCV004765940