ClinVar Miner

Submissions for variant NM_000718.4(CACNA1B):c.4584+119A>G

gnomAD frequency: 0.01314  dbSNP: rs13298580
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001786039 SCV002027795 likely benign not provided 2021-05-20 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001786039 SCV005224917 likely benign not provided criteria provided, single submitter not provided

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