ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.2125-15G>A

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Myriad Genetics, Inc. RCV004593686 SCV005082743 likely benign Familial cancer of breast 2024-05-07 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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