ClinVar Miner

Submissions for variant NM_001127222.2(CACNA1A):c.3990-36C>G

gnomAD frequency: 0.00030  dbSNP: rs371395911
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001558130 SCV001780015 likely benign not provided 2020-05-03 criteria provided, single submitter clinical testing

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