ClinVar Miner

Submissions for variant NM_001453.3(FOXC1):c.89C>T (p.Ala30Val)

dbSNP: rs1762516271
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Medical Molecular Genetics, University of Zurich RCV001250450 SCV001424839 uncertain significance Anterior segment dysgenesis 3 2019-08-01 no assertion criteria provided research

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