ClinVar Miner

Submissions for variant NM_144969.3(ZDHHC15):c.380-5del

dbSNP: rs751518520
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001528629 SCV001740658 benign not specified no assertion criteria provided clinical testing
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) RCV001573349 SCV001799104 likely benign not provided no assertion criteria provided clinical testing

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