ClinVar Miner

Submissions for variant NC_000004.12:g.93013415_93157863del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000156930 SCV000206651 pathogenic Autosomal recessive spinocerebellar ataxia 18 2013-07-01 no assertion criteria provided literature only

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