ClinVar Miner

Submissions for variant NC_000023.10:g.(?_37641330)_(37641446_?)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 RCV002040754 SCV002299773 likely pathogenic Granulomatous disease, chronic, X-linked 2020-12-06 criteria provided, single submitter clinical testing In summary, the currently available evidence indicates that the variant is pathogenic, but additional data are needed to prove that conclusively. Therefore, this variant has been classified as Likely Pathogenic. This variant disrupts the p.Gly20 amino acid residue in CYBB. Other variant(s) that disrupt this residue have been determined to be pathogenic (PMID: 9585602, 19410294, 20729109). This suggests that this residue is clinically significant, and that variants that disrupt this residue are likely to be disease-causing. This variant has not been reported in the literature in individuals with CYBB-related conditions. This variant is a gross deletion of the genomic region encompassing exon(s) 2 of the CYBB gene. This variant would be expected to be in-frame, preserving the integrity of the reading frame.

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