ClinVar Miner

Submissions for variant NM_003919.3(SGCE):c.463+17G>A

dbSNP: rs2485133908
Minimum review status: Collection method:
Minimum conflict level:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003085604 SCV003462037 likely benign Myoclonic dystonia 11 2025-10-13 criteria provided, single submitter clinical testing

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