ClinVar Miner

Submissions for variant NM_016492.5(RANGRF):c.181G>T (p.Glu61Ter)

dbSNP: rs140704891
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000171022 SCV000223586 benign not specified 2017-05-10 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Invitae RCV001842512 SCV000554077 benign Cardiac arrhythmia 2024-01-30 criteria provided, single submitter clinical testing
Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute RCV000845313 SCV000987355 likely benign not provided criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV000171022 SCV001963210 benign not specified no assertion criteria provided clinical testing
Clinical Genetics, Academic Medical Center RCV000171022 SCV001978837 benign not specified no assertion criteria provided clinical testing

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