ClinVar Miner

Submissions for variant NM_052872.4(IL17F):c.58T>C (p.Leu20=)

gnomAD frequency: 0.00001  dbSNP: rs374833689
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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 RCV001489039 SCV001693573 likely benign Candidiasis, familial, 6 2023-11-10 criteria provided, single submitter clinical testing

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