ClinVar Miner

Submissions for variant NM_000722.4(CACNA2D1):c.659-23CT[2]

dbSNP: rs66474649
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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 RCV001700851 SCV001921895 benign not specified no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001703329 SCV001932419 likely benign not provided no assertion criteria provided clinical testing

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