ClinVar Miner

Submissions for variant NM_005120.3(MED12):c.1486-13C>T

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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 RCV003776724 SCV002975859 likely benign FG syndrome 2022-07-09 criteria provided, single submitter clinical testing

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