ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.4776+23_4776+25del

dbSNP: rs770860526
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000674119 SCV000799395 likely benign Ataxia-telangiectasia syndrome 2018-04-17 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001182964 SCV001348595 likely benign Hereditary cancer-predisposing syndrome 2019-05-23 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000674119 SCV002242717 likely benign Ataxia-telangiectasia syndrome 2025-01-11 criteria provided, single submitter clinical testing

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