ClinVar Miner

Submissions for variant NM_004560.4(ROR2):c.1873G>A (p.Asp625Asn)

gnomAD frequency: 0.00003  dbSNP: rs754476697
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001365551 SCV001561826 uncertain significance not provided 2021-08-26 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002476668 SCV002801388 uncertain significance Brachydactyly type B1; Autosomal recessive Robinow syndrome 2022-02-09 criteria provided, single submitter clinical testing

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