ClinVar Miner

Submissions for variant NM_006929.5(SKIC2):c.2394G>A (p.Glu798=)

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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 RCV005146007 SCV005778083 likely benign not provided 2024-09-02 criteria provided, single submitter clinical testing

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