ClinVar Miner

Submissions for variant NM_001349338.3(FOXP1):c.1183G>A (p.Ala395Thr)

dbSNP: rs376351360
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Centre de Biologie Pathologie Génétique, Centre Hospitalier Universitaire de Lille RCV000681495 SCV000808945 likely benign Intellectual disability 2017-01-01 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002531422 SCV002987418 benign not provided 2023-06-05 criteria provided, single submitter clinical testing

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