ClinVar Miner

Submissions for variant NM_006939.4(SOS2):c.1965C>T (p.Asp655=)

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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 RCV002775548 SCV003024822 likely benign Noonan syndrome 9 2023-10-13 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003395518 SCV004134085 likely benign not provided 2023-05-01 criteria provided, single submitter clinical testing SOS2: BP4, BP7

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