ClinVar Miner

Submissions for variant NM_000890.5(KCNJ5):c.405C>T (p.Gly135=)

gnomAD frequency: 0.00003  dbSNP: rs1249014742
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000921902 SCV001067317 likely benign Long QT syndrome 2019-12-12 criteria provided, single submitter clinical testing

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