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: chr11:31794027:G>T
 
ClinVar:           chr11:31794027:G>A 		NM_001368894.2(PAX6):c.807+5C>T SNV
Conflicting classifications of pathogenicity Condition: not provided
Aniridia 1
Irido-corneo-trabecular dysgenesis		 Criteria Provided
Conflicting Classifications

4 SubmittersRCV000994594RCV001858793