ClinVar Miner

Submissions for variant NM_005120.3(MED12):c.2686-20A>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 RCV003776834 SCV002989300 likely benign FG syndrome 2023-09-15 criteria provided, single submitter clinical testing

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