ClinVar Miner

Submissions for variant NC_000023.10:g.(?_14861689)_(15870650_?)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 RCV003122594 SCV003791169 pathogenic Multiple congenital anomalies-hypotonia-seizures syndrome 2 2022-08-31 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 PIGA-related conditions. A gross deletion of the genomic region encompassing the full coding sequence of the PIGA gene has been identified. Loss-of-function variants in PIGA are known to be pathogenic (PMID: 24706016, 26545172). The boundaries of this event are unknown as they extend beyond the assayed region for this gene and therefore may encompass additional genes.

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