ClinVar Miner

Submissions for variant NM_005120.3(MED12):c.5841T>C (p.Tyr1947=)

dbSNP: rs2519715361
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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 RCV003764404 SCV004551376 likely benign FG syndrome 2023-07-17 criteria provided, single submitter clinical testing

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