ClinVar Miner

Submissions for variant NM_000719.7(CACNA1C):c.5680+15C>T (rs114036394)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000079304 SCV000111174 benign not specified 2013-10-25 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000270774 SCV000377921 likely benign Timothy syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000325771 SCV000377922 likely benign Brugada syndrome 2016-06-14 criteria provided, single submitter clinical testing
Integrated Genetics/Laboratory Corporation of America RCV000029421 SCV000052071 benign Cardiac arrhythmia 2015-04-29 no assertion criteria provided clinical testing

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