ClinVar Miner

Submissions for variant NM_005989.4(AKR1D1):c.379-4del

dbSNP: rs35402657
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001673122 SCV001883562 benign not provided 2021-06-18 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001530057 SCV001744612 benign not specified no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001673122 SCV001932783 likely benign not provided no assertion criteria provided clinical testing

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