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: chr10:47348604:C>G
 
ClinVar:           chr10:47348604:C>T 		NM_002900.3(RBP3):c.120C>T (p.Cys40=) SNV
Conflicting classifications of pathogenicity Condition: not provided
Retinitis pigmentosa
not specified		 Criteria Provided
Conflicting Classifications

3 SubmittersRCV000896345RCV001107520RCV005436281
IndiGenomes: chr10:47348783:C>G
 
ClinVar:           chr10:47348783:C>T 		NM_002900.3(RBP3):c.299C>T (p.Pro100Leu) SNV
Conflicting classifications of pathogenicity Condition: not provided Criteria Provided
Conflicting Classifications

2 SubmittersRCV000733678