ClinVar Miner

Submissions for variant NM_000064.4(C3):c.2686G>C (p.Val896Leu)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005028725 SCV005647576 uncertain significance Age related macular degeneration 9; Atypical hemolytic-uremic syndrome with C3 anomaly; Complement component 3 deficiency 2024-01-20 criteria provided, single submitter clinical testing

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