ClinVar Miner

Submissions for variant MSH6:c.3647-51_3647-35del17 (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%
Integrated Genetics/Laboratory Corporation of America RCV000074904 SCV000052936 benign Lynch syndrome 2011-01-06 no assertion criteria provided clinical testing
Mayo Clinic Genetic Testing Laboratories,Mayo Clinic RCV000202136 SCV000257271 benign not specified no assertion criteria provided research
Mayo Clinic Genetic Testing Laboratories,Mayo Clinic RCV000202136 SCV000257272 benign not specified no assertion criteria provided research

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