ClinVar Miner

Submissions for variant NM_001008537.3(NEXMIF):c.4509T>C (p.Pro1503=) (rs41303725)

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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 RCV000194878 SCV000247708 likely benign not specified 2015-12-17 criteria provided, single submitter clinical testing
Invitae RCV000549293 SCV000653831 benign Mental retardation, X-linked 98 2017-08-31 criteria provided, single submitter clinical testing

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