ClinVar Miner

Submissions for variant NM_001349338.3(FOXP1):c.1653-1G>A

dbSNP: rs1575741313
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Total submissions: 1
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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 RCV000851515 SCV000994570 pathogenic Intellectual disability-severe speech delay-mild dysmorphism syndrome 2018-07-03 criteria provided, single submitter clinical testing

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