ClinVar Miner

Submissions for variant NM_006939.4(SOS2):c.1766A>G (p.Asn589Ser)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003756181 SCV004510423 likely benign Noonan syndrome 9 2024-12-04 criteria provided, single submitter clinical testing

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