ClinVar Miner

Submissions for variant NM_006939.4(SOS2):c.3348C>T (p.Ser1116=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002958510 SCV003277939 likely benign Noonan syndrome 9 2024-12-06 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV005239562 SCV005887815 likely benign not specified 2025-01-12 criteria provided, single submitter clinical testing

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