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: chr6:35503822:G>A
 
ClinVar:           chr6:35503822:G>T 		NM_003322.6(TULP1):c.1139C>A (p.Thr380Lys) SNV
Likely pathogenic Condition: not provided Criteria Provided
Single Submitter

1 SubmittersRCV001963709