ClinVar Miner

Submissions for variant NM_018896.5(CACNA1G):c.1925-10C>T

gnomAD frequency: 0.00240  dbSNP: rs139447235
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000963369 SCV001110520 benign not provided 2025-01-13 criteria provided, single submitter clinical testing
GeneDx RCV000963369 SCV001869734 benign not provided 2021-04-22 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV000963369 SCV001931691 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV000963369 SCV001974438 likely benign not provided no assertion criteria provided clinical testing

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