ClinVar Miner

Submissions for variant NM_003108.4(SOX11):c.697G>A (p.Asp233Asn)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003715376 SCV004481248 benign not provided 2023-10-03 criteria provided, single submitter clinical testing
Clinical Genetics Laboratory, Skane University Hospital Lund RCV003715376 SCV005198318 uncertain significance not provided 2023-05-24 criteria provided, single submitter clinical testing

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