ClinVar Miner

Submissions for variant NM_005120.3(MED12):c.4806G>A (p.Ser1602=)

dbSNP: rs755218771
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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 RCV003771567 SCV001727423 benign FG syndrome 2020-08-10 criteria provided, single submitter clinical testing

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