ClinVar Miner

Submissions for variant NC_000011.9:g.(22272558_22276916)_(22284590_22291857)del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003123564 SCV003801322 likely pathogenic Autosomal recessive limb-girdle muscular dystrophy 2023-01-31 criteria provided, single submitter clinical testing Variant summary: The variant identified by MLPA or other technology involves the deletion of exons 13-17 in the ANO5 gene. A presumed nomenclature of c.(1180+1_1181-1)_(1898+1_1899-1)del has been designated for the purposes of this classification. Although exact breakpoints of this deletion are not known, it is expected to result in a frameshift in the ANO5 gene, a known mechanism of disease. The variant was absent in 21694 control chromosomes in gnomAD database (structural variants data set). Deletion of exons 13-17 has been reported in the literature in an individual affected with anoctaminopathy-5 (example: Lahoria_2014) These data indicate that the variant may be associated with disease. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar after 2014. Based on the evidence outlined above, the variant was classified as likely pathogenic.

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