ClinVar Miner

Submissions for variant NM_001349338.3(FOXP1):c.825del (p.Ser276fs)

dbSNP: rs2106870085
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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 Clinical Genetics, Copenhagen University Hospital, Rigshospitalet RCV002226945 SCV002505855 pathogenic Intellectual disability-severe speech delay-mild dysmorphism syndrome 2021-08-01 criteria provided, single submitter clinical testing

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