ClinVar Miner

Submissions for variant NM_006939.4(SOS2):c.1068+17_1068+18del

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV002308706 SCV002600834 uncertain significance not specified 2022-10-30 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005096127 SCV005793524 likely benign Noonan syndrome 9 2024-09-16 criteria provided, single submitter clinical testing

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