ClinVar Miner

Submissions for variant NM_002234.4(KCNA5):c.843G>A (p.Leu281=)

gnomAD frequency: 0.00016  dbSNP: rs755035314
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001484584 SCV001689003 likely benign Atrial fibrillation, familial, 7 2020-02-10 criteria provided, single submitter clinical testing

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