ClinVar Miner

Submissions for variant NM_004560.4(ROR2):c.2625dup (p.Thr876fs)

dbSNP: rs1836888405
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Beijing Key Laboratory for Genetic Research of Skeletal Deformity, Peking Union Medical College Hospital RCV001293680 SCV001482401 likely pathogenic Brachydactyly type B1 2019-05-31 no assertion criteria provided research
Beijing Key Laboratory for Genetic Research of Skeletal Deformity, Peking Union Medical College Hospital RCV001310271 SCV001499881 uncertain significance Short stature 2021-01-31 no assertion criteria provided research

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