ClinVar Miner

Submissions for variant NM_006363.6(SEC23B):c.*9_*10del

dbSNP: rs142180765
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000176084 SCV000227681 benign not specified 2014-12-23 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV000176084 SCV000311457 benign not specified criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000368332 SCV000433026 likely benign Congenital dyserythropoietic anemia 2016-06-14 criteria provided, single submitter clinical testing

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