ClinVar Miner

Submissions for variant NM_004560.4(ROR2):c.494+25G>A

gnomAD frequency: 0.68697  dbSNP: rs12683181
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000249961 SCV000310467 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001640532 SCV001856722 benign not provided 2018-10-16 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001795452 SCV002033675 benign Brachydactyly type B1 2021-11-07 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001795453 SCV002033676 benign Autosomal recessive Robinow syndrome 2021-11-07 criteria provided, single submitter clinical testing

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