ClinVar Miner

Submissions for variant NM_004560.4(ROR2):c.175+17A>G

gnomAD frequency: 0.00243  dbSNP: rs372392835
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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 RCV002211519 SCV002356432 benign not provided 2024-12-04 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002498205 SCV002805162 likely benign Brachydactyly type B1; Autosomal recessive Robinow syndrome 2021-08-23 criteria provided, single submitter clinical testing

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