ClinVar Miner

Submissions for variant NM_005120.3(MED12):c.1113G>A (p.Leu371=)

dbSNP: rs780470012
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000841240 SCV000983198 likely benign not provided 2019-06-14 criteria provided, single submitter clinical testing
Invitae RCV003762900 SCV003457946 benign FG syndrome 2022-07-02 criteria provided, single submitter clinical testing

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