ClinVar Miner

Submissions for variant NM_033100.4(CDHR1):c.2246_2253del (p.Arg749fs) (rs886044648)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics RCV000359142 SCV000345785 likely pathogenic not provided 2016-09-02 criteria provided, single submitter clinical testing

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