ClinVar Miner

Submissions for variant NM_001201550.3(CFHR4):c.128A>T (p.Tyr43Phe)

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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 RCV002294711 SCV002587671 likely benign Atypical hemolytic-uremic syndrome 2021-01-05 criteria provided, single submitter clinical testing

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