ClinVar Miner

Submissions for variant NM_006939.4(SOS2):c.3338-8del

dbSNP: rs2139510301
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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 RCV001456180 SCV001659957 likely benign Noonan syndrome 9 2023-03-04 criteria provided, single submitter clinical testing

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