ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.1950C>T (p.Gly650=) (rs747380250)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000550199 SCV000624706 likely benign Hereditary nonpolyposis colon cancer 2017-06-08 criteria provided, single submitter clinical testing
Color RCV000583517 SCV000690237 likely benign Hereditary cancer-predisposing syndrome 2017-10-06 criteria provided, single submitter clinical testing

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