ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.3285-13del

dbSNP: rs1245305174
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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 RCV000583650 SCV000687463 likely benign Hereditary cancer-predisposing syndrome 2017-08-21 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002060594 SCV002333643 likely benign Ataxia-telangiectasia syndrome 2025-01-22 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004592832 SCV005084079 likely benign Familial cancer of breast 2024-05-14 criteria provided, single submitter clinical testing This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing.

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