ClinVar Miner

Submissions for variant NM_001127222.2(CACNA1A):c.1199-298A>G

gnomAD frequency: 0.00300  dbSNP: rs141686642
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001585048 SCV001811210 likely benign not provided 2018-06-26 criteria provided, single submitter clinical testing

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