ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.5319+15A>G

dbSNP: rs2135916591
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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 RCV002083390 SCV002376163 likely benign Ataxia-telangiectasia syndrome 2021-07-31 criteria provided, single submitter clinical testing

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