ClinVar Miner

Submissions for variant NM_001466.4(FZD2):c.1301_1302delinsTT (p.Gly434Val)

dbSNP: rs1555657074
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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 RCV000577879 SCV000583570 likely pathogenic Autosomal dominant Robinow syndrome 2 2017-06-01 criteria provided, single submitter research

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