ClinVar Miner

Submissions for variant NM_002234.4(KCNA5):c.1596G>A (p.Pro532=)

gnomAD frequency: 0.00010  dbSNP: rs71582899
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001438034 SCV001640901 likely benign Atrial fibrillation, familial, 7 2024-01-26 criteria provided, single submitter clinical testing
GeneDx RCV001552726 SCV001773468 likely benign not provided 2019-02-19 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 24068186)

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