ClinVar Miner

Submissions for variant NM_030787.4(CFHR5):c.643T>C (p.Ser215Pro)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome Diagnostics Laboratory, The Hospital for Sick Children RCV002294687 SCV002587556 likely benign Atypical hemolytic-uremic syndrome 2022-03-15 criteria provided, single submitter clinical testing

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