ClinVar Miner

Submissions for variant NM_032588.4(TRIM63):c.*2G>A

gnomAD frequency: 0.00441  dbSNP: rs77965623
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV001702315 SCV003928622 uncertain significance not specified 2023-04-26 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003407774 SCV004123543 likely benign not provided 2023-01-01 criteria provided, single submitter clinical testing TRIM63: BS2
Breakthrough Genomics, Breakthrough Genomics RCV003407774 SCV005282193 benign not provided criteria provided, single submitter not provided
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001702315 SCV001932922 benign not specified no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001702315 SCV001955024 benign not specified no assertion criteria provided clinical testing

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