ClinVar Miner

Submissions for variant NM_005120.3(MED12):c.5749-11del

dbSNP: rs2147830057
Minimum review status: Collection method:
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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 RCV003762998 SCV002422807 benign FG syndrome 2022-11-22 criteria provided, single submitter clinical testing

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