ClinVar Miner

Submissions for variant NM_014159.7(SETD2):c.4918-78AC[17]

dbSNP: rs61571386
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000501522 SCV000597004 likely benign not specified 2016-04-29 criteria provided, single submitter clinical testing
GeneDx RCV001597149 SCV001831063 benign not provided 2019-08-15 criteria provided, single submitter clinical testing

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