ClinVar Miner

Submissions for variant NM_005751.5(AKAP9):c.1857A>G (p.Glu619=)

dbSNP: rs2130666228
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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 RCV001427272 SCV001629947 likely benign Long QT syndrome 2022-11-01 criteria provided, single submitter clinical testing

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