ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.1875C>A (p.Ser625=) (rs63749886)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000166130 SCV000216901 likely benign Hereditary cancer-predisposing syndrome 2014-10-15 criteria provided, single submitter clinical testing
Color RCV000166130 SCV000908384 likely benign Hereditary cancer-predisposing syndrome 2018-05-29 criteria provided, single submitter clinical testing

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