ClinVar Miner

Submissions for variant NM_005120.3(MED12):c.2685+17G>T

gnomAD frequency: 0.00005  dbSNP: rs767584131
Minimum review status: Collection method:
Minimum conflict level:
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 RCV003762178 SCV002379761 benign FG syndrome 2024-06-05 criteria provided, single submitter clinical testing

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