ClinVar Miner

Submissions for variant NM_005120.3(MED12):c.3355-16_3355-13del

dbSNP: rs1556336608
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 RCV002251375 SCV000722617 likely benign not provided 2022-05-25 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.
Labcorp Genetics (formerly Invitae), Labcorp RCV003767593 SCV002930271 likely benign FG syndrome 2022-08-29 criteria provided, single submitter clinical testing

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