ClinVar Miner

Submissions for variant NM_006767.4(LZTR1):c.2326-10G>A

dbSNP: rs778909787
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002219657 SCV002377355 likely benign not provided 2024-12-29 criteria provided, single submitter clinical testing
GeneDx RCV002219657 SCV004036522 uncertain significance not provided 2023-03-20 criteria provided, single submitter clinical testing Not observed at significant frequency in large population cohorts (gnomAD); In silico analysis supports that this variant does not alter splicing; Has not been previously published as pathogenic or benign to our knowledge

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