ClinVar Miner

Submissions for variant NM_000249.4(MLH1):c.-29G>C

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Myriad Genetics, Inc. RCV005246222 SCV005895003 benign Colorectal cancer, hereditary nonpolyposis, type 2 2024-11-19 criteria provided, single submitter clinical testing This variant is considered benign. This variant occurs in the non-coding 5' untranslated region of the gene, and is not expected to impact protein function.

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