ClinVar Miner

Submissions for variant NM_032776.3(JMJD1C):c.168+10_168+11delinsCG

dbSNP: rs34353506
Minimum review status: Collection method:
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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 RCV000556415 SCV000632276 benign Early myoclonic encephalopathy 2025-02-04 criteria provided, single submitter clinical testing

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