ClinVar Miner

Submissions for variant NM_033400.3(ZFHX2):c.6034G>A (p.Glu2012Lys)

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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 Hospital of Duesseldorf RCV003459030 SCV004177246 uncertain significance Indifference to pain, congenital, autosomal dominant criteria provided, single submitter not provided

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