ClinVar Miner

Submissions for variant NM_001378457.1(DMXL2):c.1617+20T>C

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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 RCV005064558 SCV005722113 likely benign not provided 2024-05-16 criteria provided, single submitter clinical testing

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