ClinVar Miner

Submissions for variant NM_002439.5(MSH3):c.-34_-10dup

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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. RCV003459141 SCV004185943 benign Familial adenomatous polyposis 4 2023-11-06 criteria provided, single submitter clinical testing This variant is considered benign. This variant is intronic and is not expected to impact mRNA splicing.

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