ClinVar Miner

Submissions for variant GRCh37/hg19 2p21(chr2:47511660-47641537)x1

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Medicover Genetics GmbH, Medicover Humangenetik Berlin-Lichtenberg MVZ RCV003230305 SCV003926649 pathogenic Lynch syndrome 1 2023-05-26 no assertion criteria provided clinical testing

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