ClinVar Miner

Submissions for variant NM_006939.4(SOS2):c.2958+12C>A

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV005234735 SCV005876283 likely benign Noonan syndrome 9 2023-12-15 criteria provided, single submitter clinical testing

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