ClinVar Miner

Submissions for variant NM_004560.4(ROR2):c.1100A>T (p.Asn367Ile)

dbSNP: rs2118683614
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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 RCV001353123 SCV001441488 likely pathogenic Autosomal recessive Robinow syndrome 2020-04-02 no assertion criteria provided research

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