ClinVar Miner

Submissions for variant NM_002234.4(KCNA5):c.744C>G (p.Ser248=)

dbSNP: rs1040705459
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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 RCV002103378 SCV002384830 likely benign Atrial fibrillation, familial, 7 2021-02-23 criteria provided, single submitter clinical testing

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