ClinVar Miner

Submissions for variant NM_000535.7(PMS2):c.24-2A>C

dbSNP: rs1583419860
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Leipzig Medical Center RCV001253267 SCV001428894 pathogenic Mismatch repair cancer syndrome 1 2018-05-02 criteria provided, single submitter clinical testing

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