ClinVar Miner

Submissions for variant NM_000249.3(MLH1):c.1191G>A (p.Leu397=) (rs35164771)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000165602 SCV000216336 likely benign Hereditary cancer-predisposing syndrome 2014-08-26 criteria provided, single submitter clinical testing
Invitae RCV000536405 SCV000625047 likely benign Hereditary nonpolyposis colorectal neoplasms 2019-12-31 criteria provided, single submitter clinical testing
Color RCV000165602 SCV000684726 likely benign Hereditary cancer-predisposing syndrome 2017-06-08 criteria provided, single submitter clinical testing
Integrated Genetics/Laboratory Corporation of America RCV001193242 SCV001361970 likely benign not specified 2019-10-31 criteria provided, single submitter clinical testing

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