ClinVar Miner

Submissions for variant NM_005216.5(DDOST):c.1063+34dup

dbSNP: rs11428148
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
GeneDx RCV001643902 SCV001856098 benign not provided 2018-06-23 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001658368 SCV001876596 benign Congenital disorder of glycosylation type Ir 2021-07-30 criteria provided, single submitter clinical testing

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