ClinVar Miner

Submissions for variant NM_005120.3(MED12):c.6411C>T (p.Phe2137=)

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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 RCV003763452 SCV004469318 benign FG syndrome 2023-06-21 criteria provided, single submitter clinical testing

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