ClinVar Miner

Submissions for variant GRCh37/hg19 4p11(chr4:48784236-48907733)x3

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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 RCV001004817 SCV001164310 uncertain significance Anophthalmia; Renal hypoplasia/aplasia 2019-07-08 no assertion criteria provided clinical testing

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