ClinVar Miner

Submissions for variant MSH6:c.3647-51_3647-35del17

dbSNP: rs267607687
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
International Society for Gastrointestinal Hereditary Tumours (InSiGHT) RCV000074904 SCV000108116 likely benign Lynch syndrome 2013-09-05 reviewed by expert panel research Intronic variant with no effect on splicing & MAF 0.01-1%
GeneDx RCV001675601 SCV001895254 benign not provided 2018-06-23 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV000074904 SCV000052936 benign Lynch syndrome 2011-01-06 no assertion criteria provided clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000202136 SCV000257271 benign not specified no assertion criteria provided research

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