ClinVar Miner

Submissions for variant NM_002234.4(KCNA5):c.1828G>A (p.Glu610Lys)

gnomAD frequency: 0.00003  dbSNP: rs121908593
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000014414 SCV000034663 pathogenic Atrial fibrillation, familial, 7 2009-05-01 no assertion criteria provided literature only

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