ClinVar Miner

Submissions for variant NM_000719.7(CACNA1C):c.2854-11C>G

dbSNP: rs2153406175
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Al Jalila Children’s Genomics Center, Al Jalila Childrens Speciality Hospital RCV002477909 SCV002774987 uncertain significance not provided 2022-12-17 criteria provided, single submitter clinical testing
Al Jalila Children’s Genomics Center, Al Jalila Childrens Speciality Hospital RCV001733516 SCV001984033 uncertain significance Brugada syndrome 3 2021-03-01 flagged submission clinical testing

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