ClinVar Miner

Submissions for variant NM_020699.4(GATAD2B):c.1390G>A (p.Ala464Thr)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Genetics Laboratory, University Hospital Schleswig-Holstein RCV002291113 SCV002583355 uncertain significance Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome 2021-12-01 no assertion criteria provided clinical testing

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