ClinVar Miner

Submissions for variant NM_032682.5(FOXP1):c.1540C>T (p.Arg514Cys) (rs869025203)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Language and Genetics Department,Max Planck Institute for Psycholinguistics RCV000207490 SCV000246200 pathogenic Mental retardation with language impairment and with or without autistic features 2015-01-01 criteria provided, single submitter clinical testing
OMIM RCV000207490 SCV000502987 pathogenic Mental retardation with language impairment and with or without autistic features 2019-05-07 no assertion criteria provided literature only

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