ClinVar Miner

Submissions for variant NM_002234.4(KCNA5):c.464A>G (p.Tyr155Cys)

gnomAD frequency: 0.00007  dbSNP: rs202117321
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Biesecker Lab/Clinical Genomics Section, National Institutes of Health RCV000171649 SCV000050680 uncertain significance not provided 2013-06-24 criteria provided, single submitter research
Mendelics RCV000988774 SCV001138631 uncertain significance Atrial fibrillation, familial, 7 2019-05-28 criteria provided, single submitter clinical testing
Invitae RCV000988774 SCV001655145 likely benign Atrial fibrillation, familial, 7 2023-08-30 criteria provided, single submitter clinical testing

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