ClinVar Miner

Submissions for variant NM_001376.5(DYNC1H1):c.5292C>G (p.Thr1764=)

dbSNP: rs755482182
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV001817355 SCV002065532 likely benign not specified 2017-12-01 criteria provided, single submitter clinical testing

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