ClinVar Miner

Submissions for variant NM_001111125.3(IQSEC2):c.2617C>A (p.Arg873Ser)

dbSNP: rs782383669
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Leipzig Medical Center RCV001800266 SCV002044459 uncertain significance Intellectual disability, X-linked 1 2021-12-20 criteria provided, single submitter clinical testing
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center RCV005232663 SCV005874077 uncertain significance not provided 2024-10-21 criteria provided, single submitter clinical testing PM2, BP4, PP2

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