ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.457+52T>A (rs3136282)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
International Society for Gastrointestinal Hereditary Tumours (InSiGHT) RCV000074995 SCV000108213 no known pathogenicity Lynch syndrome 2013-09-05 reviewed by expert panel research MAF >1%
Counsyl RCV000412274 SCV000488266 benign Hereditary nonpolyposis colorectal cancer type 5 2016-02-10 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV001001447 SCV001158688 benign not specified 2018-07-02 criteria provided, single submitter clinical testing

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