ClinVar Miner

Submissions for variant NM_002234.4(KCNA5):c.543C>T (p.Ser181=)

gnomAD frequency: 0.00001  dbSNP: rs750031654
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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 RCV001469353 SCV001673433 likely benign Atrial fibrillation, familial, 7 2022-06-11 criteria provided, single submitter clinical testing

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