ClinVar Miner

Submissions for variant NM_002439.5(MSH3):c.792+50G>A

gnomAD frequency: 0.03852  dbSNP: rs6151630
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
GeneDx RCV001707120 SCV001935238 benign not provided 2018-06-22 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002268563 SCV002550478 benign not specified 2025-03-04 criteria provided, single submitter clinical testing

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