ClinVar Miner

Submissions for variant NM_006939.4(SOS2):c.859-19T>C

dbSNP: rs1435577590
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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 RCV002093581 SCV002382452 likely benign Noonan syndrome 9 2023-12-25 criteria provided, single submitter clinical testing

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