ClinVar Miner

Submissions for variant GRCh37/hg19 12p13.33(chr12:1345909-1476210)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 Goettingen RCV000787287 SCV000926223 likely pathogenic Delayed speech and language development 2019-04-04 no assertion criteria provided clinical testing

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