ClinVar Miner

Submissions for variant NM_005751.5(AKAP9):c.1647G>A (p.Gln549=)

dbSNP: rs991776167
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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 RCV001462232 SCV001666145 likely benign Long QT syndrome 2018-04-12 criteria provided, single submitter clinical testing

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