ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.7749A>T (p.Ile2583=)

dbSNP: rs2136526242
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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 RCV001494498 SCV001699156 likely benign Ataxia-telangiectasia syndrome 2019-05-12 criteria provided, single submitter clinical testing

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