ClinVar Miner

Submissions for variant NM_002439.5(MSH3):c.3000+9C>T

dbSNP: rs2112106737
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002128033 SCV002442524 likely benign not provided 2024-03-07 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV003493920 SCV004243210 likely benign not specified 2025-03-04 criteria provided, single submitter clinical testing

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