ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.1235+11A>G

dbSNP: rs2135296543
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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 RCV002081191 SCV002372503 likely benign Ataxia-telangiectasia syndrome 2021-08-12 criteria provided, single submitter clinical testing

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