ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.260+22C>G (rs55927047)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
International Society for Gastrointestinal Hereditary Tumours (InSiGHT) RCV000074760 SCV000107970 no known pathogenicity Lynch syndrome 2013-09-05 reviewed by expert panel research MAF >1%
Color Health, Inc RCV000584553 SCV000690272 benign Hereditary cancer-predisposing syndrome 2017-07-12 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV000202025 SCV001158692 benign not specified 2018-07-02 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000202025 SCV000257224 benign not specified no assertion criteria provided clinical testing
Department of Pathology and Laboratory Medicine,Sinai Health System RCV001353436 SCV000592565 uncertain significance not provided no assertion criteria provided clinical testing

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