ClinVar Miner

Submissions for variant NM_005666.4(CFHR2):c.213G>A (p.Thr71=)

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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 RCV002294698 SCV002587607 benign Atypical hemolytic-uremic syndrome 2022-07-08 criteria provided, single submitter clinical testing

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