ClinVar Miner

Submissions for variant NM_199437.2(PRDM10):c.2018G>A (p.Cys673Tyr)

dbSNP: rs1319176059
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV001579510 SCV001807506 uncertain significance not provided no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001579510 SCV001953469 uncertain significance not provided no assertion criteria provided clinical testing

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