ClinVar Miner

Submissions for variant NM_004560.4(ROR2):c.899G>T (p.Cys300Phe)

dbSNP: rs2118699409
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Lupski Lab, Baylor-Hopkins CMG, Baylor College of Medicine RCV001353132 SCV001441500 likely pathogenic Autosomal recessive Robinow syndrome no assertion criteria provided research

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