ClinVar Miner

Submissions for variant NM_000051.3(ATM):c.3285-5T>C (rs876659715)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000214287 SCV000276472 likely benign Hereditary cancer-predisposing syndrome 2019-11-18 criteria provided, single submitter clinical testing Insufficient or conflicting evidence
Color Health, Inc RCV000214287 SCV000913997 uncertain significance Hereditary cancer-predisposing syndrome 2018-12-20 criteria provided, single submitter clinical testing
Invitae RCV001417887 SCV001620095 likely benign Ataxia-telangiectasia syndrome 2020-07-19 criteria provided, single submitter clinical testing

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