ClinVar Miner

Submissions for variant NM_001126108.2(SLC12A3):c.659del (p.Gly220fs)

dbSNP: rs2144689577
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Diagnostics Laboratory, M Health Fairview: University of Minnesota RCV001526394 SCV001736728 pathogenic Familial hypokalemia-hypomagnesemia 2021-03-26 criteria provided, single submitter clinical testing

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