ClinVar Miner

Submissions for variant NM_001111125.3(IQSEC2):c.3054G>A (p.Thr1018=)

dbSNP: rs782748833
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Research Center, Shahid Beheshti University of Medical Sciences RCV000626231 SCV000746878 uncertain significance Intellectual disability, X-linked 1 2017-12-18 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000626231 SCV001732683 benign Intellectual disability, X-linked 1 2022-10-07 criteria provided, single submitter clinical testing

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