ClinVar Miner

Submissions for variant NM_000092.5(COL4A4):c.2165-13del

dbSNP: rs140965334
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000350906 SCV000428105 likely benign Alport syndrome 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV001519571 SCV001728460 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
GeneDx RCV001519571 SCV001847890 benign not provided 2018-07-31 criteria provided, single submitter clinical testing

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