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: chr4:125318625:C>A
 
ClinVar:           chr4:125318625:C>A 		NM_001291303.3(FAT4):c.2214C>A (p.Val738=) SNV
Conflicting classifications of pathogenicity Condition: not provided
FAT4-related disorder		 Criteria Provided
Conflicting Classifications

2 SubmittersRCV002650501RCV003395501