ClinVar Miner

Submissions for variant GRCh37/hg19 12p12.1(chr12:23723120-23908799)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 for Human Genetics, University Hospital Essen RCV000857284 SCV000999876 pathogenic Lamb-Shaffer syndrome 2019-08-05 no assertion criteria provided clinical testing

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