ClinVar Miner

Submissions for variant NM_000251.2(MSH2):c.741C>G (p.Gly247=) (rs747321505)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000197277 SCV000253161 likely benign Hereditary nonpolyposis colorectal neoplasms 2019-12-31 criteria provided, single submitter clinical testing
Color RCV000774558 SCV000908283 likely benign Hereditary cancer-predisposing syndrome 2018-03-12 criteria provided, single submitter clinical testing

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