ClinVar Miner

Submissions for variant NM_000064.4(C3):c.1352A>G (p.Asn451Ser)

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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 RCV005015932 SCV005649918 uncertain significance Age related macular degeneration 9; Atypical hemolytic-uremic syndrome with C3 anomaly; Complement component 3 deficiency 2024-02-07 criteria provided, single submitter clinical testing

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