ClinVar Miner

Submissions for variant NM_002234.4(KCNA5):c.1608G>A (p.Lys536=)

gnomAD frequency: 0.00001  dbSNP: rs1271807597
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 RCV001425769 SCV001628407 likely benign Atrial fibrillation, familial, 7 2019-04-05 criteria provided, single submitter clinical testing

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