ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.628-56C>T

gnomAD frequency: 0.11629  dbSNP: rs1800936
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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) RCV000075012 SCV000108232 no known pathogenicity Lynch syndrome 2013-09-05 reviewed by expert panel research MAF >1%
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000202203 SCV001158694 benign not specified 2018-07-02 criteria provided, single submitter clinical testing
GeneDx RCV001650892 SCV001865793 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000202203 SCV000257303 benign not specified no assertion criteria provided research

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