ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.1508C>T (p.Ser503Phe) (rs63750897)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color RCV000773432 SCV000907126 uncertain significance Hereditary cancer-predisposing syndrome 2018-07-05 criteria provided, single submitter clinical testing
Mendelics RCV000986715 SCV001135806 uncertain significance Hereditary nonpolyposis colorectal cancer type 5 2019-05-28 criteria provided, single submitter clinical testing

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