ClinVar Miner

Submissions for variant NM_007366.5(PLA2R1):c.3316G>A (p.Gly1106Ser)

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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 RCV002294692 SCV002587577 benign Atypical hemolytic-uremic syndrome 2022-10-05 criteria provided, single submitter clinical testing

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