ClinVar Miner

Submissions for variant NM_201596.3(CACNB2):c.120+338T>C

dbSNP: rs751631146
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Genetics, Academic Medical Center RCV001700615 SCV001924614 benign not specified no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001727949 SCV001968925 likely benign not provided no assertion criteria provided clinical testing

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