ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.8584+16A>C

dbSNP: rs1322889530
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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 RCV000581410 SCV000687842 likely benign Hereditary cancer-predisposing syndrome 2017-08-11 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002061696 SCV002487024 likely benign Ataxia-telangiectasia syndrome 2023-02-28 criteria provided, single submitter clinical testing

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