ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.8952G>T (p.Leu2984=)

dbSNP: rs2137884197
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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 RCV002110344 SCV002436942 likely benign Ataxia-telangiectasia syndrome 2020-12-25 criteria provided, single submitter clinical testing

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