ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.5859A>G (p.Thr1953=)

dbSNP: rs1555110429
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000583162 SCV000687646 likely benign Hereditary cancer-predisposing syndrome 2017-10-23 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002060614 SCV002358763 likely benign Ataxia-telangiectasia syndrome 2024-01-28 criteria provided, single submitter clinical testing

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