ClinVar Miner

Submissions for variant NM_006416.5(SLC35A1):c.752-157_752-156insCTCA

dbSNP: rs10638303
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001659682 SCV001874336 benign not provided 2021-05-15 criteria provided, single submitter clinical testing
OMIM RCV000005115 SCV000025292 risk factor CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIf, MODIFIER OF 2005-04-01 no assertion criteria provided literature only

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