ClinVar Miner

Submissions for variant NM_000251.2(MSH2):c.1830C>T (p.His610=) (rs766326295)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000469892 SCV000559206 likely benign Hereditary nonpolyposis colorectal neoplasms 2019-12-31 criteria provided, single submitter clinical testing
Ambry Genetics RCV000570499 SCV000662232 likely benign Hereditary cancer-predisposing syndrome 2015-03-30 criteria provided, single submitter clinical testing
Color RCV000570499 SCV000684981 likely benign Hereditary cancer-predisposing syndrome 2016-11-01 criteria provided, single submitter clinical testing
Integrated Genetics/Laboratory Corporation of America RCV001174849 SCV001338239 likely benign not specified 2020-02-08 criteria provided, single submitter clinical testing

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