ClinVar Miner

Submissions for variant NM_001040108.2(MLH3):c.3280+19T>C

gnomAD frequency: 0.00001  dbSNP: rs773682420
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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 RCV002095155 SCV002384052 likely benign Colorectal cancer, hereditary nonpolyposis, type 7 2024-02-20 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002268611 SCV002551421 likely benign not specified 2025-03-04 criteria provided, single submitter clinical testing

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