ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.4002-13_4002-10dup

dbSNP: rs59056100
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
International Society for Gastrointestinal Hereditary Tumours (InSiGHT) RCV000074980 SCV000108195 no known pathogenicity Lynch syndrome 2013-09-05 reviewed by expert panel research MAF >1%
Quest Diagnostics Nichols Institute San Juan Capistrano RCV003477464 SCV004222033 benign not provided 2023-08-11 criteria provided, single submitter clinical testing

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