ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.6095+17T>C

dbSNP: rs2136122949
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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 RCV002201950 SCV002495080 likely benign Ataxia-telangiectasia syndrome 2023-02-16 criteria provided, single submitter clinical testing

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