ClinVar Miner

Submissions for variant NM_001349338.3(FOXP1):c.1652+540G>A

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV002512230 SCV002821200 likely benign not provided 2024-08-01 criteria provided, single submitter clinical testing FOXP1: BS1
PreventionGenetics, part of Exact Sciences RCV003961061 SCV004771812 benign FOXP1-related disorder 2020-11-10 no assertion criteria provided clinical testing This variant is classified as benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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