ClinVar Miner

Submissions for variant NM_005472.5(KCNE3):c.*920_*922dup

dbSNP: rs60016728
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
Illumina Laboratory Services, Illumina RCV000340003 SCV000374041 uncertain significance Brugada syndrome 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004693062 SCV005190467 uncertain significance not provided criteria provided, single submitter not provided

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