ClinVar Miner

Submissions for variant NM_001040108.2(MLH3):c.402A>G (p.Glu134=)

dbSNP: rs545763648
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000655412 SCV000777342 likely benign Colorectal cancer, hereditary nonpolyposis, type 7 2017-10-16 criteria provided, single submitter clinical testing

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