ClinVar Miner

Submissions for variant NM_006939.4(SOS2):c.2022A>G (p.Arg674=)

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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 RCV003074359 SCV003454573 likely benign Noonan syndrome 9 2023-12-31 criteria provided, single submitter clinical testing

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