ClinVar Miner

Submissions for variant NM_005751.5(AKAP9):c.1242C>T (p.Phe414=)

dbSNP: rs200250245
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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 RCV002055005 SCV002493235 benign Long QT syndrome 2021-09-21 criteria provided, single submitter clinical testing

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