ClinVar Miner

Submissions for variant NM_181798.1(KCNQ1):c.37A>G (p.Ser13Gly) (rs120074192)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Cardiovascular Biomedical Research Unit,Royal Brompton & Harefield NHS Foundation Trust RCV000057673 SCV000089192 not provided Atrial fibrillation no assertion provided literature only This variant has been reported as associated with Atrial fibrillation in the following publications (PMID:12522251;PMID:15368194;PMID:17467630;PMID:18599533;PMID:21224508;PMID:22250012;PMID:17999538;PMID:22508963). This is a literature report, and does not necessarily reflect the clinical interpretation of the Imperial College / Royal Brompton Cardiovascular Genetics laboratory.
OMIM RCV000003293 SCV000023451 pathogenic Atrial fibrillation, familial, 3 2003-01-10 no assertion criteria provided literature only

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