ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.2234T>A (p.Ile745Asn)

dbSNP: rs1558664787
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
International Society for Gastrointestinal Hereditary Tumours (InSiGHT) RCV000680208 SCV000807672 likely pathogenic Lynch syndrome 1 2018-06-13 reviewed by expert panel curation Multifactorial likelihood analysis posterior probability > 0.95 (0.964)

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