ClinVar Miner

Submissions for variant NM_006939.4(SOS2):c.3076-19T>C

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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 RCV003231023 SCV003928316 uncertain significance not specified 2023-04-23 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003779843 SCV004694941 likely benign Noonan syndrome 9 2023-10-22 criteria provided, single submitter clinical testing

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