ClinVar Miner

Submissions for variant GRCh37/hg19 10q25.1(chr10:107722094-109081424)x3

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Reutter Lab, Institute of Human Genetics, University Hospital Bonn RCV000524033 SCV000537149 likely benign VATER association no assertion criteria provided research

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