ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.4008T>G (p.Val1336=) (rs1553333982)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000536364 SCV000624961 likely benign Hereditary nonpolyposis colon cancer 2017-06-09 criteria provided, single submitter clinical testing
Color RCV000583268 SCV000690434 likely benign Hereditary cancer-predisposing syndrome 2016-11-14 criteria provided, single submitter clinical testing

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