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: chr17:42911016:G>A
 
ClinVar:           chr17:42911016:G>A 		NM_000151.4(G6PC1):c.664G>A (p.Gly222Arg) SNV
Pathogenic Glycogen storage disease due to glucose-6-phosphatase deficiency type IA Criteria Provided
Multiple Submitters
No Conflicts

3 SubmittersRCV001235195