ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.4062G>T (p.Leu1354=) (rs863224335)

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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 RCV000219894 SCV000275180 likely benign Hereditary cancer-predisposing syndrome 2015-04-21 criteria provided, single submitter clinical testing
Counsyl RCV000409551 SCV000488350 likely benign Hereditary nonpolyposis colorectal cancer type 5 2016-03-03 criteria provided, single submitter clinical testing
Color RCV000219894 SCV000690437 likely benign Hereditary cancer-predisposing syndrome 2017-08-02 criteria provided, single submitter clinical testing
Invitae RCV000630392 SCV000751348 likely benign not provided 2018-12-22 criteria provided, single submitter clinical testing

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