ClinVar Miner

Submissions for variant NM_005591.4(MRE11):c.20+16C>T

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV005085246 SCV005713664 likely benign Ataxia-telangiectasia-like disorder 2024-08-08 criteria provided, single submitter clinical testing

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