ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.3168G>C (p.Val1056=) (rs1553414594)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000533692 SCV000624824 likely benign Hereditary nonpolyposis colon cancer 2017-05-22 criteria provided, single submitter clinical testing
Color RCV000777192 SCV000912883 likely benign Hereditary cancer-predisposing syndrome 2018-08-28 criteria provided, single submitter clinical testing

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