ClinVar Miner

Submissions for variant NM_000091.4(COL4A3):c.4380T>C (p.Cys1460=) (rs114430490)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000250210 SCV000302077 likely benign not specified criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000710821 SCV000841126 benign not provided 2018-08-20 criteria provided, single submitter clinical testing
Invitae RCV000710821 SCV001024368 benign not provided 2020-11-27 criteria provided, single submitter clinical testing
Natera, Inc. RCV001273242 SCV001456039 benign Alport syndrome 2020-09-16 no assertion criteria provided clinical testing

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