ClinVar Miner

Submissions for variant NM_000249.4(MLH1):c.546-15_546-12del

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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 RCV003760279 SCV004525101 likely benign Hereditary nonpolyposis colorectal neoplasms 2023-01-27 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV005249630 SCV005895252 likely benign Colorectal cancer, hereditary nonpolyposis, type 2 2024-11-19 criteria provided, single submitter clinical testing This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing.

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