ClinVar Miner

Submissions for variant NM_004560.4(ROR2):c.2724C>T (p.Thr908=)

gnomAD frequency: 0.00004  dbSNP: rs374824850
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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 RCV002179412 SCV002339792 likely benign not provided 2024-10-30 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002494038 SCV002802902 likely benign Brachydactyly type B1; Autosomal recessive Robinow syndrome 2021-12-15 criteria provided, single submitter clinical testing

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