ClinVar Miner

Submissions for variant NM_006363.6(SEC23B):c.1233+25dup

dbSNP: rs57738665
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000389743 SCV000433012 benign Congenital dyserythropoietic anemia 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001709607 SCV001937545 benign not provided 2021-05-24 criteria provided, single submitter clinical testing

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