ClinVar Miner

Submissions for variant NM_000891.3(KCNJ2):c.-163_-162insTC

gnomAD frequency: 0.02248  dbSNP: rs61077847
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001684907 SCV001903599 benign not provided 2019-11-14 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002496006 SCV002798007 likely benign Andersen Tawil syndrome; Short QT syndrome type 3; Atrial fibrillation, familial, 9 2021-10-08 criteria provided, single submitter clinical testing

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