ClinVar Miner

Submissions for variant NM_020680.4(SCYL1):c.1507T>C (p.Cys503Arg) (rs374754187)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Biochemical Molecular Genetic Laboratory,King Abdulaziz Medical City RCV000985231 SCV001133265 uncertain significance Spinocerebellar ataxia, autosomal recessive 21 2019-09-26 no assertion criteria provided clinical testing

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