ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.8010+18C>A

dbSNP: rs2086560371
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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 RCV002108071 SCV002395199 likely benign Ataxia-telangiectasia syndrome 2022-07-07 criteria provided, single submitter clinical testing

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