ClinVar Miner

Submissions for variant GRCh37/hg19 2p21(chr2:47612218-47693997)x1

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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 RCV003329521 SCV004036106 pathogenic Hereditary nonpolyposis colorectal neoplasms 2022-10-11 criteria provided, single submitter clinical testing

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