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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