ClinVar Miner

Submissions for variant NM_020381.4(PDSS2):c.290C>T (p.Thr97Ile)

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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 RCV002294732 SCV002587775 uncertain significance Kidney disorder 2017-01-23 criteria provided, single submitter clinical testing

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