ClinVar Miner

Submissions for variant NM_001451.3(FOXF1):c.658G>T (p.Gly220Cys) (rs752504125)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Reutter Lab, Institute of Human Genetics, University Hospital Bonn RCV000201858 SCV000222774 likely pathogenic VATER association 2015-01-01 criteria provided, single submitter research

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