ClinVar Miner

Submissions for variant NM_001349338.3(FOXP1):c.1146+19C>G

gnomAD frequency: 0.00228  dbSNP: rs140060227
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics RCV000514403 SCV000610079 likely benign not provided 2017-08-24 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000514403 SCV002392465 benign not provided 2024-01-29 criteria provided, single submitter clinical testing

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