ClinVar Miner

Submissions for variant NC_000015.9:g.(?_42676661)_(42686559_?)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 RCV001956448 SCV002243680 pathogenic Autosomal recessive limb-girdle muscular dystrophy type 2A 2024-01-07 criteria provided, single submitter clinical testing This variant is a gross deletion of the genomic region encompassing exon(s) 2-8 of the CAPN3 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 CAPN3 are known to be pathogenic (PMID: 10330340, 15689361). A similar copy number variant has been observed in individual(s) with autosomal recessive limb-girdle muscular dystrophy (PMID: 17318636, 17979987, 21896784). In at least one individual the data is consistent with being in trans (on the opposite chromosome) from a pathogenic variant. For these reasons, this variant has been classified as Pathogenic.

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