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:85978857:C>G
 
ClinVar:           chrX:85978857:C>T 		NM_000390.4(CHM):c.224G>A (p.Trp75Ter) SNV
Pathogenic Condition: not provided
Choroideremia		 Criteria Provided
Multiple Submitters
No Conflicts

2 SubmittersRCV001386911RCV005002013