ClinVar Miner

Submissions for variant NM_000891.3(KCNJ2):c.774C>T (p.Ile258=)

dbSNP: rs1057524125
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001698368 SCV000534620 likely benign not provided 2018-11-29 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002063604 SCV002385062 likely benign Andersen Tawil syndrome; Short QT syndrome type 3 2023-08-04 criteria provided, single submitter clinical testing

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