ClinVar Miner

Submissions for variant NM_000091.4(COL4A3):c.1398T>C (p.Asp466=) (rs145833114)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000250473 SCV000302060 likely benign not specified criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000710809 SCV000841114 benign not provided 2018-08-20 criteria provided, single submitter clinical testing
Invitae RCV000710809 SCV001032295 benign not provided 2020-12-07 criteria provided, single submitter clinical testing
GeneDx RCV000710809 SCV001869794 benign not provided 2019-01-25 criteria provided, single submitter clinical testing
Natera, Inc. RCV001273237 SCV001456030 benign Alport syndrome 2020-09-16 no assertion criteria provided clinical testing

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