ClinVar Miner

Submissions for variant NM_004153.4(ORC1):c.2405A>G (p.His802Arg)

dbSNP: rs587780411
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000117875 SCV000152147 uncertain significance not provided 2014-01-17 criteria provided, single submitter clinical testing
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre RCV004813059 SCV005438119 uncertain significance Meier-Gorlin syndrome 1 2024-12-17 criteria provided, single submitter clinical testing

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