ClinVar Miner

Submissions for variant NM_002234.4(KCNA5):c.1149T>C (p.Gly383=) (rs2359641)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Diagnostic Laboratory, Department of Genetics,University Medical Center Groningen RCV000600992 SCV000733177 benign Atrial fibrillation, familial, 7 no assertion criteria provided clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000395109 SCV000379701 likely benign Familial atrial fibrillation 2016-06-14 criteria provided, single submitter clinical testing
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000251000 SCV000539416 benign not specified 2016-03-28 criteria provided, single submitter clinical testing Variant identified in a genome or exome case(s) and assessed due to predicted null impact of the variant or pathogenic assertions in the literature or databases. Disclaimer: This variant has not undergone full assessment. The following are preliminary notes: MAF
PreventionGenetics RCV000251000 SCV000308775 benign not specified criteria provided, single submitter clinical testing

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