ClinVar Miner

Submissions for variant NM_001142966.3(GREB1L):c.2614_2615del (p.Leu872fs)

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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 Medical Genetics and Applied Genomics, University Hospital Tübingen RCV003154319 SCV003842317 pathogenic Renal hypodysplasia/aplasia 3 2023-03-22 criteria provided, single submitter clinical testing

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