ClinVar Miner

Submissions for variant NM_000091.5(COL4A3):c.1368T>C (p.Tyr456=)

dbSNP: rs766591906
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 RCV000979517 SCV001127461 likely benign not provided 2023-10-13 criteria provided, single submitter clinical testing
Natera, Inc. RCV001832272 SCV002076396 likely benign Alport syndrome 2020-11-04 no assertion criteria provided clinical testing

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