ClinVar Miner

Submissions for variant NM_032776.3(JMJD1C):c.5241C>T (p.His1747=)

dbSNP: rs1845896422
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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 RCV001437927 SCV001640793 likely benign Early myoclonic encephalopathy 2020-03-06 criteria provided, single submitter clinical testing

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