ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.3078-16A>C

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003123398 SCV003800800 uncertain significance not specified 2023-01-10 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003500805 SCV004353605 likely benign Ataxia-telangiectasia syndrome 2023-09-06 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004593211 SCV005082491 likely benign Familial cancer of breast 2024-05-13 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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