ClinVar Miner

Submissions for variant NM_002234.4(KCNA5):c.1662G>C (p.Arg554=)

dbSNP: rs2137773916
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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 RCV001403272 SCV001605137 likely benign Atrial fibrillation, familial, 7 2022-03-18 criteria provided, single submitter clinical testing

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