ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.3792A>C (p.Leu1264=) (rs786202051)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000196734 SCV000253112 likely benign not provided 2018-06-07 criteria provided, single submitter clinical testing
Counsyl RCV000408977 SCV000489234 likely benign Hereditary nonpolyposis colorectal cancer type 5 2016-09-06 criteria provided, single submitter clinical testing
Ambry Genetics RCV000565750 SCV000662557 likely benign Hereditary cancer-predisposing syndrome 2017-03-07 criteria provided, single submitter clinical testing Synonymous alterations with insufficient evidence to classify as benign

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