ClinVar Miner

Submissions for variant NM_000535.7(PMS2):c.23+21_23+28del

dbSNP: rs1554308880
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Pathology and Laboratory Medicine, Sinai Health System RCV000503298 SCV000592916 likely pathogenic Lynch syndrome criteria provided, single submitter clinical testing

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