ClinVar Miner

Submissions for variant NM_005120.3(MED12):c.4416-6C>T

gnomAD frequency: 0.00004  dbSNP: rs775717904
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003761373 SCV001705734 likely benign FG syndrome 2024-08-01 criteria provided, single submitter clinical testing

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