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: chr14:45181636:G>A
 
ClinVar:           chr14:45181636:G>A 		NM_020937.4(FANCM):c.4318-1G>A SNV
Conflicting classifications of pathogenicity Fanconi anemia
Condition: not provided		 Criteria Provided
Conflicting Classifications

3 SubmittersRCV001233917RCV001773527