ClinVar Miner

Submissions for variant NM_007366.5(PLA2R1):c.816T>C (p.Asp272=)

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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 RCV002294611 SCV002587174 likely benign Kidney disorder 2016-12-12 criteria provided, single submitter clinical testing

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