ClinVar Miner

Submissions for variant NM_000091.5(COL4A3):c.3956-8_3956-5del

dbSNP: rs779522146
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
Illumina Laboratory Services, Illumina RCV000288326 SCV000428187 uncertain significance Alport syndrome 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002057674 SCV002440509 likely benign not provided 2024-02-05 criteria provided, single submitter clinical testing

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