ClinVar Miner

Submissions for variant NM_016032.4(ZDHHC9):c.167+10G>A (rs140526450)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics RCV000177289 SCV000229133 benign not specified 2014-07-21 criteria provided, single submitter clinical testing
Invitae RCV000646768 SCV000768553 benign Mental retardation, X-linked, syndromic, Raymond type 2019-12-31 criteria provided, single submitter clinical testing

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