ClinVar Miner

Submissions for variant NM_005751.5(AKAP9):c.3426T>C (p.Ala1142=)

dbSNP: rs758236336
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002125159 SCV002445020 likely benign Long QT syndrome 2021-01-01 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV003138090 SCV003823094 uncertain significance Long QT syndrome 11 2021-10-18 criteria provided, single submitter clinical testing

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