ClinVar Miner

Submissions for variant NM_000891.3(KCNJ2):c.*2758T>C

gnomAD frequency: 0.04554  dbSNP: rs1324652195
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001663326 SCV001873589 benign not provided 2021-05-13 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002501998 SCV002807523 benign Andersen Tawil syndrome; Short QT syndrome type 3; Atrial fibrillation, familial, 9 2021-08-17 criteria provided, single submitter clinical testing

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