ClinVar Miner

Submissions for variant NM_030787.4(CFHR5):c.759T>G (p.Asp253Glu)

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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 RCV004794262 SCV005412647 uncertain significance not provided 2024-08-28 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005006563 SCV005633990 uncertain significance C3 glomerulonephritis 2024-03-02 criteria provided, single submitter clinical testing

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