ClinVar Miner

Submissions for variant NM_032682.5(FOXP1):c.622C>T (p.Gln208Ter) (rs1553709881)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000595726 SCV000703984 pathogenic not provided 2016-11-28 criteria provided, single submitter clinical testing
Dobyns Lab,Seattle Children's Research Institute RCV000779638 SCV000916315 pathogenic Mental retardation with language impairment and with or without autistic features; Cerebellar vermis hypoplasia 2019-02-18 no assertion criteria provided research

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