ClinVar Miner

Submissions for variant NM_002026.3(FN1):c.1070G>A (p.Gly357Glu) (rs140926439)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000974439 SCV001122262 likely benign not provided 2020-11-18 criteria provided, single submitter clinical testing
Cavalleri Lab, Royal College of Surgeons in Ireland RCV001171320 SCV001328267 uncertain significance Chronic kidney disease 2020-05-28 criteria provided, single submitter research PP2, PP3, BS1
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV000974439 SCV001743758 likely benign not provided no assertion criteria provided clinical testing

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