ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.8301T>G (p.Leu2767=)

dbSNP: rs1060504303
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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 RCV001443466 SCV001646438 likely benign Ataxia-telangiectasia syndrome 2016-04-09 criteria provided, single submitter clinical testing

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