ClinVar Miner

Submissions for variant NM_015046.7(SETX):c.3182C>T (p.Pro1061Leu) (rs12352982)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000557872 SCV000645248 benign Amyotrophic lateral sclerosis type 4; Spinocerebellar ataxia autosomal recessive 1 2017-10-23 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000713203 SCV000843789 benign not provided 2017-09-13 criteria provided, single submitter clinical testing

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