ClinVar Miner

Submissions for variant NM_006939.4(SOS2):c.2356C>T (p.Leu786=)

dbSNP: rs1884611451
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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 RCV002159145 SCV002473403 likely benign Noonan syndrome 9 2021-07-07 criteria provided, single submitter clinical testing

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