ClinVar Miner

Submissions for variant NM_001349338.3(FOXP1):c.282+16777A>G

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre RCV003989960 SCV004806104 uncertain significance Intellectual disability-severe speech delay-mild dysmorphism syndrome 2024-03-25 criteria provided, single submitter clinical testing

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