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: chr2:31373872:C>T
 
ClinVar:           chr2:31373872:C>G 		NM_000379.4(XDH):c.1686+1G>C SNV
Conflicting classifications of pathogenicity Hereditary xanthinuria type 1
Xanthinuria type II
Condition: not provided
XDH-related disorder		 Criteria Provided
Conflicting Classifications

7 SubmittersRCV000616942RCV000685712RCV003156264RCV004730996
IndiGenomes: chr2:31373894:T>TG
 
ClinVar:           chr2:31373894:T>TG 		NM_000379.4(XDH):c.1664dup (p.Ala556fs) Duplication
Pathogenic Xanthinuria type II Criteria Provided
Single Submitter

1 SubmittersRCV002944197