ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.5496+18T>G

dbSNP: rs2135931607
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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 RCV002213048 SCV002368360 likely benign Ataxia-telangiectasia syndrome 2024-04-24 criteria provided, single submitter clinical testing

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