ClinVar Miner

Submissions for variant NM_012200.4(B3GAT3):c.909+270_909+271del

dbSNP: rs549953964
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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 RCV001529142 SCV001742118 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001727870 SCV001972635 benign not specified no assertion criteria provided clinical testing

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