ClinVar Miner

Submissions for variant NC_000010.10:g.(?_90749963)_(90750683_?)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 RCV001975215 SCV002242601 pathogenic Autoimmune lymphoproliferative syndrome type 1 2022-06-28 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 FAS-related conditions. This variant is a gross deletion of the genomic region encompassing exon(s) 1 of the FAS gene, which includes the initiator codon. This deletion extends beyond the assayed region for this gene and therefore may encompass additional genes. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in FAS are known to be pathogenic (PMID: 10875918, 22237435).

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