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: chr19:6718117:G>A
 
ClinVar:           chr19:6718117:G>A 		NM_000064.4(C3):c.481C>T (p.Arg161Trp) SNV
Pathogenic Condition: not provided
Atypical hemolytic-uremic syndrome with C3 anomaly		 Criteria Provided
Multiple Submitters
No Conflicts

4 SubmittersRCV001507921RCV002466678