ClinVar Miner

Submissions for variant NM_006939.4(SOS2):c.3338-6C>G

gnomAD frequency: 0.00001  dbSNP: rs749149552
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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 RCV001203051 SCV001374197 likely benign Noonan syndrome 9 2022-11-15 criteria provided, single submitter clinical testing

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