ClinVar Miner

Submissions for variant NM_000091.5(COL4A3):c.1167C>G (p.Gly389=)

dbSNP: rs2070734491
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001499537 SCV001704301 likely benign not provided 2023-07-19 criteria provided, single submitter clinical testing
Natera, Inc. RCV001278692 SCV001465722 uncertain significance Alport syndrome 2020-08-13 no assertion criteria provided clinical testing

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