ClinVar Miner

Submissions for variant NC_000021.9:g.(?_46111467)_(46121133_?)del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001032779 SCV001196086 pathogenic Bethlem myopathy 1 2019-05-01 criteria provided, single submitter clinical testing This variant is a gross deletion of the genomic region encompassing exons 2-17 of the COL6A2 gene, which includes the initiator codon. The 5' end of this event is unknown as it extends beyond the assayed region for this gene and therefore may encompass additional genes. The 3' boundary is likely confined to intron 17 of the COL6A2 gene. This is expected to result in an absent or disrupted protein product. This variant has not been reported in the literature in individuals with COL6A2-related disease. Loss-of-function variants in COL6A2 are known to be pathogenic (PMID: 19884007, 20976770). For these reasons, this variant has been classified as Pathogenic.

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