ClinVar Miner

Submissions for variant NM_001040108.1(MLH3):c.1870G>C (p.Glu624Gln) (rs28756986)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000232137 SCV000285761 benign MLH3-Related Lynch Syndrome 2018-01-09 criteria provided, single submitter clinical testing
OMIM RCV000005899 SCV000026081 uncertain significance Hereditary nonpolyposis colorectal cancer type 7 2009-04-01 no assertion criteria provided literature only

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