ClinVar Miner

Submissions for variant NM_001365792.1(DAB1):c.43G>A (p.Ala15Thr)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV003145976 SCV003830401 uncertain significance Spinocerebellar ataxia type 37 2020-03-09 criteria provided, single submitter clinical testing

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