ClinVar Miner

Submissions for variant NM_000535.7(PMS2):c.*92dup

dbSNP: rs267608145
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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) RCV000076783 SCV000108271 no known pathogenicity Lynch syndrome 2013-09-05 reviewed by expert panel research MAF >1%
GeneDx RCV001540228 SCV001758088 benign not provided 2018-12-06 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001540228 SCV002058087 benign not provided 2023-11-30 criteria provided, single submitter clinical testing

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