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: chr17:19661241:G>A
 
ClinVar:           chr17:19661241:G>T 		NM_000382.3(ALDH3A2):c.913G>T (p.Glu305Ter) SNV
Likely pathogenic Sjögren-Larsson syndrome Criteria Provided
Single Submitter

1 SubmittersRCV002306488