ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.2839-13C>T

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002857889 SCV003228546 likely benign Ataxia-telangiectasia syndrome 2023-06-25 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004593081 SCV005081916 likely benign Familial cancer of breast 2024-05-10 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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