ClinVar Miner

Submissions for variant NM_000051.3(ATM):c.7905C>T (p.Ala2635=) (rs757829783)

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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 RCV000561940 SCV000665395 likely benign Hereditary cancer-predisposing syndrome 2017-07-28 criteria provided, single submitter clinical testing
Color RCV000561940 SCV000904739 likely benign Hereditary cancer-predisposing syndrome 2018-10-19 criteria provided, single submitter clinical testing
Invitae RCV000628211 SCV000749105 likely benign Ataxia-telangiectasia syndrome 2018-01-08 criteria provided, single submitter clinical testing

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