ClinVar Miner

Submissions for variant NM_004082.5(DCTN1):c.1855-7C>T

dbSNP: rs2103634309
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001425318 SCV001627945 likely benign Amyotrophic lateral sclerosis type 1; Perry syndrome; Neuronopathy, distal hereditary motor, type 7B 2019-02-03 criteria provided, single submitter clinical testing

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