ClinVar Miner

Submissions for variant NM_005120.3(MED12):c.3609C>T (p.Cys1203=)

gnomAD frequency: 0.00001  dbSNP: rs751742488
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 RCV001721828 SCV001948625 benign not provided 2021-06-20 criteria provided, single submitter clinical testing
Invitae RCV003761417 SCV003247135 benign FG syndrome 2023-08-23 criteria provided, single submitter clinical testing

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