ClinVar Miner

Submissions for variant NM_001127222.2(CACNA1A):c.2737_2739delinsTCT (p.Pro913Ser) (rs886043758)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics RCV000401942 SCV000341867 likely benign not specified 2016-06-04 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000991664 SCV001143316 benign not provided 2018-11-28 criteria provided, single submitter clinical testing
GeneDx RCV000991664 SCV001851334 benign not provided 2016-10-20 criteria provided, single submitter clinical testing

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