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: chrX:153743670:G>A
 
ClinVar:           chrX:153743670:G>A 		NM_000033.4(ABCD1):c.2173G>A (p.Ala725Thr) SNV
Conflicting classifications of pathogenicity not specified
Condition: not provided
Adrenoleukodystrophy		 Criteria Provided
Conflicting Classifications

3 SubmittersRCV000426538RCV003488588RCV002524859