ClinVar Miner

Submissions for variant NM_020381.4(PDSS2):c.31C>T (p.Pro11Ser)

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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 RCV002294658 SCV002587421 uncertain significance Focal segmental glomerulosclerosis 2019-11-01 criteria provided, single submitter clinical testing

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