ClinVar Miner

Submissions for variant NM_000051.3(ATM):c.2377-5T>C (rs754206007)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000572482 SCV000665314 uncertain significance Hereditary cancer-predisposing syndrome 2017-03-03 criteria provided, single submitter clinical testing Insufficient evidence
Invitae RCV000628280 SCV000749175 likely benign Ataxia-telangiectasia syndrome 2017-12-17 criteria provided, single submitter clinical testing

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