ClinVar Miner

Submissions for variant NM_000249.4(MLH1):c.1667+15T>C

dbSNP: rs1474788239
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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 RCV002165473 SCV002339217 likely benign Hereditary nonpolyposis colorectal neoplasms 2024-11-16 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV003493911 SCV004243147 likely benign not specified 2025-03-04 criteria provided, single submitter clinical testing

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