ClinVar Miner

Submissions for variant NM_021224.6(ZNF462):c.4784A>G (p.His1595Arg)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV004576000 SCV005050491 uncertain significance not provided 2024-05-01 criteria provided, single submitter clinical testing ZNF462: PM2:Supporting

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