ClinVar Miner

Submissions for variant NM_001376.5(DYNC1H1):c.3804G>A (p.Thr1268=) (rs757595764)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000501838 SCV000594412 uncertain significance not specified 2016-08-22 criteria provided, single submitter clinical testing
CeGaT Praxis fuer Humangenetik Tuebingen RCV000658704 SCV000780490 uncertain significance not provided 2018-03-31 criteria provided, single submitter clinical testing

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