ClinVar Miner

Submissions for variant NM_004560.4(ROR2):c.1184-1G>T

dbSNP: rs2118645585
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet RCV002226817 SCV002505694 pathogenic Autosomal recessive Robinow syndrome 2021-08-01 criteria provided, single submitter clinical testing

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