ClinVar Miner

Submissions for variant NM_000890.5(KCNJ5):c.810T>C (p.Leu270=)

dbSNP: rs7118824
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001464246 SCV001668212 likely benign Long QT syndrome 2020-03-09 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002506537 SCV002809194 likely benign Long QT syndrome 13; Familial hyperaldosteronism type III 2022-03-03 criteria provided, single submitter clinical testing

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