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: chr4:102529852:C>T
 
ClinVar:           chr4:102529852:C>T 		NM_003998.4(NFKB1):c.56C>T (p.Pro19Leu) SNV
Conflicting classifications of pathogenicity Inborn genetic diseases
Condition: not provided		 Criteria Provided
Conflicting Classifications

2 SubmittersRCV002823470RCV003435905