ClinVar Miner

Submissions for variant NM_018319.3(TDP1):c.-276_-274dupCCG (rs35210768)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000395896 SCV000389379 benign Autosomal recessive cerebellar ataxia 2016-06-14 criteria provided, single submitter clinical testing

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