ClinVar Miner

Submissions for variant NM_003394.4(WNT10B):c.901C>T (p.Pro301Ser)

gnomAD frequency: 0.01260  dbSNP: rs35034312
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000964427 SCV001111633 benign not provided 2024-01-29 criteria provided, single submitter clinical testing
GeneDx RCV000964427 SCV001856957 benign not provided 2020-08-11 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 20579865, 16477437, 23104151)
PreventionGenetics, part of Exact Sciences RCV003916155 SCV004733736 benign WNT10B-related disorder 2019-06-26 criteria provided, single submitter clinical testing This variant is classified as benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) RCV000964427 SCV001799793 likely benign not provided no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001724198 SCV001953406 benign not specified no assertion criteria provided clinical testing

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