ClinVar Miner

Submissions for variant NM_024411.4(PDYN):c.-381A>G

gnomAD frequency: 0.49716  dbSNP: rs1997794
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000273681 SCV000433073 benign Autosomal dominant cerebellar ataxia 2016-06-14 criteria provided, single submitter clinical testing

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