ClinVar Miner

Submissions for variant GRCh37/hg19 2q21.1(chr2:132140614-132312325)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 RCV000519182 SCV000537141 likely benign VATER association no assertion criteria provided research

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