ClinVar Miner

Submissions for variant NM_030787.4(CFHR5):c.1697C>T (p.Pro566Leu)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mayo Clinic Laboratories, Mayo Clinic RCV004794290 SCV005412736 uncertain significance not provided 2023-08-09 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005006565 SCV005634443 uncertain significance C3 glomerulonephritis 2023-12-27 criteria provided, single submitter clinical testing

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