ClinVar Miner

Submissions for variant NC_000018.9:g.(?_29078205)_(29102222_?)del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV004579809 SCV005063807 pathogenic Arrhythmogenic right ventricular dysplasia 10 2022-03-05 criteria provided, single submitter clinical testing For these reasons, this variant has been classified as Pathogenic. This variant has not been reported in the literature in individuals affected with DSG2-related conditions. This variant is a gross deletion of the genomic region encompassing exon(s) 1-6 of the DSG2 gene, which includes the initiator codon. This deletion extends beyond the assayed region for this gene and therefore may encompass additional genes. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in DSG2 are known to be pathogenic (PMID: 17105751, 31386562).

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