ClinVar Miner

Submissions for variant NM_004560.4(ROR2):c.174A>G (p.Lys58=)

dbSNP: rs886042213
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000370250 SCV000332572 uncertain significance not provided 2015-06-23 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005049511 SCV005677755 uncertain significance Brachydactyly type B1; Autosomal recessive Robinow syndrome 2024-01-04 criteria provided, single submitter clinical testing

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