ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.4437-7dup

dbSNP: rs1565460797
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000776669 SCV000912293 uncertain significance Hereditary cancer-predisposing syndrome 2018-10-28 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002535573 SCV003330165 likely benign Ataxia-telangiectasia syndrome 2023-11-13 criteria provided, single submitter clinical testing

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