ClinVar Miner

Submissions for variant NC_000011.10:g.(?_119028174)_(119029389_?)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 RCV000824664 SCV000965571 pathogenic Glucose-6-phosphate transport defect 2019-07-12 criteria provided, single submitter clinical testing This variant is a gross deletion of the genomic region encompassing exons 3-4 of the SLC37A4 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 4 of the SLC37A4 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 SLC37A4-related disease. Loss-of-function variants in SLC37A4 are known to be pathogenic (PMID: 9758626, 10940311). For these reasons, this variant has been classified as Pathogenic.

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