ClinVar Miner

Submissions for variant NM_000249.4(MLH1):c.1039-8_1039-7insTTTTTTA

dbSNP: rs535965616
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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 RCV000200697 SCV000252639 benign Hereditary nonpolyposis colorectal neoplasms 2023-12-24 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003430752 SCV004149364 uncertain significance not provided 2023-08-01 criteria provided, single submitter clinical testing MLH1: PM2, BP4

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