ClinVar Miner

Submissions for variant NM_006939.4(SOS2):c.2959-16A>G

gnomAD frequency: 0.00006  dbSNP: rs147830734
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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 RCV001779509 SCV002015039 benign not specified 2021-10-02 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002074069 SCV002411852 likely benign Noonan syndrome 9 2024-01-24 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002074069 SCV002763017 benign Noonan syndrome 9 criteria provided, single submitter clinical testing

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