ClinVar Miner

Submissions for variant NM_001324418.2(ADAM22):c.1981dup (p.Met661fs)

dbSNP: rs1842129329
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
New York Genome Center RCV001281452 SCV001468760 likely pathogenic Seizure; Intellectual disability 2019-09-13 criteria provided, single submitter clinical testing

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