ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.7629+12_7629+15del

dbSNP: rs1555124156
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000583525 SCV000687781 likely benign Hereditary cancer-predisposing syndrome 2017-04-06 criteria provided, single submitter clinical testing
Mendelics RCV000709191 SCV000838593 uncertain significance Ataxia-telangiectasia syndrome 2018-07-02 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000709191 SCV002391290 likely benign Ataxia-telangiectasia syndrome 2024-05-15 criteria provided, single submitter clinical testing

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