ClinVar Miner

Submissions for variant NM_002234.4(KCNA5):c.291G>A (p.Glu97=)

dbSNP: rs2137771577
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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 RCV001493832 SCV001698472 likely benign Atrial fibrillation, familial, 7 2021-09-25 criteria provided, single submitter clinical testing

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