ClinVar Miner

Submissions for variant NM_001451.3(FOXF1):c.*1176del

dbSNP: rs397854726
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000271929 SCV000399230 uncertain significance Alveolar capillary dysplasia with pulmonary venous misalignment 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000271929 SCV000399232 benign Alveolar capillary dysplasia with pulmonary venous misalignment 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001636904 SCV001848131 benign not provided 2021-05-19 criteria provided, single submitter clinical testing

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