ClinVar Miner

Submissions for variant NM_152594.3(SPRED1):c.823G>T (p.Asp275Tyr)

dbSNP: rs780737673
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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 RCV001813723 SCV002060924 uncertain significance Noonan syndrome and Noonan-related syndrome 2019-08-01 criteria provided, single submitter clinical testing

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