ClinVar Miner

Submissions for variant NM_004560.4(ROR2):c.854A>G (p.Lys285Arg)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Division of Genetics, Dept of Pediatrics, All India Institute of Medical Sciences RCV003228722 SCV003925543 likely pathogenic Autosomal recessive Robinow syndrome criteria provided, single submitter research

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