ClinVar Miner

Submissions for variant NM_001165963.4(SCN1A):c.2043+2T>C

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetics and Genomic Medicine Centre, NeuroGen Healthcare, NeuroGen Healthcare RCV004573135 SCV004175166 pathogenic not provided 2023-02-15 no assertion criteria provided clinical testing

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