ClinVar Miner

Submissions for variant NM_001369369.1(FOXN1):c.786C>T (p.Thr262=)

gnomAD frequency: 0.00007  dbSNP: rs779732404
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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 RCV001417909 SCV001620118 likely benign T-cell immunodeficiency, congenital alopecia, and nail dystrophy 2024-01-16 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004704539 SCV005212374 likely benign not provided criteria provided, single submitter not provided

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