ClinVar Miner

Submissions for variant NM_001369369.1(FOXN1):c.348C>G (p.Leu116=)

dbSNP: rs2069725069
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002210451 SCV002493329 likely benign T-cell immunodeficiency, congenital alopecia, and nail dystrophy 2021-01-17 criteria provided, single submitter clinical testing

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