ClinVar Miner

Submissions for variant NM_001349338.3(FOXP1):c.142G>C (p.Ala48Pro)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003100504 SCV003484514 benign not provided 2022-10-05 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003100504 SCV004150483 uncertain significance not provided 2023-10-01 criteria provided, single submitter clinical testing FOXP1: PM2, BP4

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