ClinVar Miner

Submissions for variant NM_014491.4(FOXP2):c.1937A>G (p.Asn646Ser)

gnomAD frequency: 0.00026  dbSNP: rs145154396
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000976028 SCV001123923 likely benign not provided 2018-10-17 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002503111 SCV002807998 likely benign Childhood apraxia of speech 2021-10-14 criteria provided, single submitter clinical testing
Centre de Biologie Pathologie Génétique, Centre Hospitalier Universitaire de Lille RCV001251758 SCV001427500 likely benign Intellectual disability 2019-01-01 no assertion criteria provided clinical testing

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