ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.3560_3563del (p.Glu1187fs)

dbSNP: rs2104521805
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetics and Molecular Pathology, SA Pathology RCV002272678 SCV002556680 pathogenic Lynch syndrome 5 2022-02-15 criteria provided, single submitter clinical testing

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