ClinVar Miner

Submissions for variant NM_181332.3(NLGN4X):c.542C>T (p.Thr181Ile)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Genetics, Rouen University Hospital, Normandy Center for Genomic and Personalized Medicine RCV003128023 SCV003804097 uncertain significance Autism spectrum disorder 2021-02-17 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003435980 SCV004164200 uncertain significance not provided 2023-10-01 criteria provided, single submitter clinical testing NLGN4X: PM2

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