ClinVar Miner

Submissions for variant NM_001451.3(FOXF1):c.276G>A (p.Trp92Ter)

dbSNP: rs2143184846
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Diagnostics Laboratory, M Health Fairview: University of Minnesota RCV001731125 SCV001981530 pathogenic Alveolar capillary dysplasia with pulmonary venous misalignment 2021-07-01 criteria provided, single submitter clinical testing

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