ClinVar Miner

Submissions for variant NM_004168.4(SDHA):c.622-13del

dbSNP: rs3835068
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000250828 SCV000310003 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001675727 SCV001893585 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV000250828 SCV001743647 benign not specified no assertion criteria provided clinical testing
Clinical Genetics Laboratory, Department of Pathology, Netherlands Cancer Institute RCV000250828 SCV001906254 benign not specified no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001675727 SCV001931754 likely benign not provided no assertion criteria provided clinical testing

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