ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.2745C>G (p.Ala915=) (rs876658904)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000213745 SCV000274743 likely benign Hereditary cancer-predisposing syndrome 2015-03-26 criteria provided, single submitter clinical testing
Invitae RCV000926509 SCV001072072 likely benign not provided 2019-02-18 criteria provided, single submitter clinical testing
Mayo Clinic Genetic Testing Laboratories,Mayo Clinic RCV000584010 SCV000691931 likely benign not specified no assertion criteria provided clinical testing

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