ClinVar Miner

Submissions for variant NM_005120.3(MED12):c.841C>T (p.Leu281Phe)

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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 RCV005111554 SCV005731780 likely benign FG syndrome 2024-08-13 criteria provided, single submitter clinical testing

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