ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.4002-10delT (rs59056100)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
DNA and Cytogenetics Diagnostics Unit,Erasmus Medical Center RCV000610486 SCV000744304 benign Hereditary nonpolyposis colorectal cancer type 5 2015-09-21 criteria provided, single submitter clinical testing
Department of Pathology and Laboratory Medicine,Sinai Health System RCV000500093 SCV000592668 benign not specified 2015-09-03 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics,University Medical Center Groningen RCV000610486 SCV000734223 benign Hereditary nonpolyposis colorectal cancer type 5 no assertion criteria provided clinical testing
International Society for Gastrointestinal Hereditary Tumours (InSiGHT) RCV000074976 SCV000108192 likely benign Lynch syndrome 2013-09-05 reviewed by expert panel research Intronic variant with no effect on splicing & MAF 0.01-1%
Mayo Clinic Genetic Testing Laboratories,Mayo Clinic RCV000500093 SCV000691944 benign not specified no assertion criteria provided clinical testing

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