ClinVar Miner

Submissions for variant NM_006939.4(SOS2):c.2057+20T>G

gnomAD frequency: 0.00001  dbSNP: rs778661549
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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 RCV003050887 SCV003444183 likely benign Noonan syndrome 9 2024-07-23 criteria provided, single submitter clinical testing

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