ClinVar Miner

Submissions for variant NC_000005.9:g.(?_78251098)_(78265035_?)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 RCV004578920 SCV005067658 pathogenic Mucopolysaccharidosis type 6 2023-10-19 criteria provided, single submitter clinical testing This variant is a gross deletion of the genomic region encompassing exon(s) 2-4 of the ARSB gene. This deletion is out-of-frame, and is expected to create a premature termination codon and result in an absent or disrupted protein product. Loss-of-function variants in ARSB are known to be pathogenic (PMID: 17458871, 22133300). This variant has not been reported in the literature in individuals affected with ARSB-related conditions. For these reasons, this variant has been classified as Pathogenic.

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