ClinVar Miner

Submissions for variant NM_000535.7(PMS2):c.576T>C (p.Cys192=)

dbSNP: rs1554302497
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000551816 SCV000625669 likely benign Hereditary nonpolyposis colorectal neoplasms 2023-12-10 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001189639 SCV001356966 likely benign Hereditary cancer-predisposing syndrome 2019-11-08 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV003320675 SCV004025128 likely benign not specified 2023-08-15 criteria provided, single submitter clinical testing

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