ClinVar Miner

Submissions for variant NM_001042517.2(DIAPH3):c.3028-4_3028-3insGTAA (rs10665848)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001697365 SCV000716968 benign not provided 2018-06-12 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV000606432 SCV000733367 benign Auditory neuropathy, autosomal dominant, 1 no assertion criteria provided clinical testing

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