ClinVar Miner

Submissions for variant NM_001098511.3(KIF2A):c.334G>A (p.Val112Met)

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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 RCV003991689 SCV004809818 uncertain significance Complex cortical dysplasia with other brain malformations 3 2024-04-04 criteria provided, single submitter clinical testing

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