ClinVar Miner

Submissions for variant NM_006939.4(SOS2):c.813C>T (p.Ser271=)

gnomAD frequency: 0.00001  dbSNP: rs371598827
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV001174922 SCV001338359 likely benign not specified 2020-02-13 criteria provided, single submitter clinical testing
Invitae RCV001485596 SCV001690034 likely benign Noonan syndrome 9 2023-10-24 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001485596 SCV002763111 likely benign Noonan syndrome 9 criteria provided, single submitter clinical testing

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