ClinVar Miner

Submissions for variant NM_030787.4(CFHR5):c.1615T>G (p.Phe539Val)

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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 RCV003481580 SCV004224756 uncertain significance not provided 2022-10-27 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005012988 SCV005634411 uncertain significance C3 glomerulonephritis 2024-01-23 criteria provided, single submitter clinical testing

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