ClinVar Miner

Submissions for variant NM_001369369.1(FOXN1):c.124-9T>C

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003861559 SCV004668883 likely benign T-cell immunodeficiency, congenital alopecia, and nail dystrophy 2023-12-29 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004703338 SCV005212371 likely benign not provided criteria provided, single submitter not provided

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