ClinVar Miner

Submissions for variant NM_000091.5(COL4A3):c.2184G>A (p.Glu728=)

dbSNP: rs779837475
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001462765 SCV001666691 likely benign not provided 2023-11-25 criteria provided, single submitter clinical testing
Natera, Inc. RCV001826291 SCV002076406 likely benign Alport syndrome 2021-07-01 no assertion criteria provided clinical testing

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