ClinVar Miner

Submissions for variant NM_001190274.2(FBXO11):c.1042-1G>A

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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 RCV004813452 SCV005438384 likely pathogenic Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities 2024-12-18 criteria provided, single submitter clinical testing

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